CN112851710B - 1-磷杂降冰片烯类手性膦催化剂、其合成方法及应用 - Google Patents
1-磷杂降冰片烯类手性膦催化剂、其合成方法及应用 Download PDFInfo
- Publication number
- CN112851710B CN112851710B CN202110018741.2A CN202110018741A CN112851710B CN 112851710 B CN112851710 B CN 112851710B CN 202110018741 A CN202110018741 A CN 202110018741A CN 112851710 B CN112851710 B CN 112851710B
- Authority
- CN
- China
- Prior art keywords
- reaction
- iii
- catalyst
- phenyl
- compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 40
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 title claims abstract description 34
- 229910000073 phosphorus hydride Inorganic materials 0.000 title claims abstract description 17
- 238000001308 synthesis method Methods 0.000 title claims abstract description 8
- 238000006243 chemical reaction Methods 0.000 claims abstract description 44
- -1 monosubstituted phenyl Chemical group 0.000 claims abstract description 23
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 18
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims abstract description 7
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 24
- 150000001875 compounds Chemical class 0.000 claims description 18
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 11
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 11
- 239000002994 raw material Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 7
- 238000004440 column chromatography Methods 0.000 claims description 6
- 239000000047 product Substances 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- 238000003756 stirring Methods 0.000 claims description 6
- 238000005406 washing Methods 0.000 claims description 6
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 claims description 5
- 238000001035 drying Methods 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 5
- 238000000926 separation method Methods 0.000 claims description 5
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 claims description 4
- 239000003153 chemical reaction reagent Substances 0.000 claims description 4
- 239000011261 inert gas Substances 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
- 239000007868 Raney catalyst Substances 0.000 claims description 3
- 229910000564 Raney nickel Inorganic materials 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 238000001704 evaporation Methods 0.000 claims description 3
- 238000011049 filling Methods 0.000 claims description 3
- 238000001914 filtration Methods 0.000 claims description 3
- 239000012044 organic layer Substances 0.000 claims description 3
- 239000007818 Grignard reagent Substances 0.000 claims description 2
- 239000013067 intermediate product Substances 0.000 claims description 2
- 238000013508 migration Methods 0.000 claims description 2
- 230000005012 migration Effects 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 238000010791 quenching Methods 0.000 claims description 2
- 230000000171 quenching effect Effects 0.000 claims description 2
- 230000002194 synthesizing effect Effects 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 abstract description 20
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract description 18
- 239000011574 phosphorus Substances 0.000 abstract description 18
- 125000001624 naphthyl group Chemical group 0.000 abstract description 9
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 abstract description 3
- 238000007363 ring formation reaction Methods 0.000 abstract description 2
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 abstract 1
- 239000007787 solid Substances 0.000 description 14
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 7
- 241000761456 Nops Species 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000006555 catalytic reaction Methods 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 230000002950 deficient Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000003446 ligand Substances 0.000 description 3
- 150000003413 spiro compounds Chemical class 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 238000006352 cycloaddition reaction Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 125000004437 phosphorous atom Chemical group 0.000 description 2
- 230000006340 racemization Effects 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- PYOKUURKVVELLB-UHFFFAOYSA-N trimethyl orthoformate Chemical compound COC(OC)OC PYOKUURKVVELLB-UHFFFAOYSA-N 0.000 description 2
- KJPRLNWUNMBNBZ-QPJJXVBHSA-N (E)-cinnamaldehyde Chemical compound O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 description 1
- UOXJNGFFPMOZDM-UHFFFAOYSA-N 2-[di(propan-2-yl)amino]ethylsulfanyl-methylphosphinic acid Chemical compound CC(C)N(C(C)C)CCSP(C)(O)=O UOXJNGFFPMOZDM-UHFFFAOYSA-N 0.000 description 1
- SFHYNDMGZXWXBU-LIMNOBDPSA-N 6-amino-2-[[(e)-(3-formylphenyl)methylideneamino]carbamoylamino]-1,3-dioxobenzo[de]isoquinoline-5,8-disulfonic acid Chemical compound O=C1C(C2=3)=CC(S(O)(=O)=O)=CC=3C(N)=C(S(O)(=O)=O)C=C2C(=O)N1NC(=O)N\N=C\C1=CC=CC(C=O)=C1 SFHYNDMGZXWXBU-LIMNOBDPSA-N 0.000 description 1
- JMEOVIGYWMBYIU-ICRZHJLGSA-N CC(C)(C)C1=CC=C([C@@H](C([C@H]([C@@](C)(C2)C(C)=C3C4=CC=CC=C4)C4=CC=CC=C4)[P@@]23=S)NS(C(C)(C)C)=O)C=C1 Chemical compound CC(C)(C)C1=CC=C([C@@H](C([C@H]([C@@](C)(C2)C(C)=C3C4=CC=CC=C4)C4=CC=CC=C4)[P@@]23=S)NS(C(C)(C)C)=O)C=C1 JMEOVIGYWMBYIU-ICRZHJLGSA-N 0.000 description 1
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 238000011914 asymmetric synthesis Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229940117916 cinnamic aldehyde Drugs 0.000 description 1
- KJPRLNWUNMBNBZ-UHFFFAOYSA-N cinnamic aldehyde Natural products O=CC=CC1=CC=CC=C1 KJPRLNWUNMBNBZ-UHFFFAOYSA-N 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000012011 nucleophilic catalyst Substances 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000009790 rate-determining step (RDS) Methods 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6568—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms
- C07F9/65683—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms the ring phosphorus atom being part of a phosphine
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
- B01J31/0255—Phosphorus containing compounds
- B01J31/0267—Phosphines or phosphonium compounds, i.e. phosphorus bonded to at least one carbon atom, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, the other atoms bonded to phosphorus being either carbon or hydrogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B53/00—Asymmetric syntheses
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/96—Spiro-condensed ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6568—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms
- C07F9/65685—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms the ring phosphorus atom being part of a phosphine oxide or thioxide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/584—Recycling of catalysts
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
本发明公开了1‑磷杂降冰片烯类手性膦催化剂、其合成方法及应用。所述催化剂的结构如下式III和III’所示：
；式中，Ar为苯基、取代苯基、萘基、取代萘基；优选的，Ar为苯基、单取代苯基、萘基；更优选的，Ar为苯基、4‑单取代苯基、2‑萘基；更进一步优选的，Ar为苯基、4‑甲基苯基、4‑甲氧基苯基、4‑苄基苯基、4‑叔丁基苯基、4‑叔丁氧基苯基苯基、2‑萘基。本发明提供的催化剂作为一类结构新颖的手性膦催化剂，通过刚性骨架的引入，形成三个完全束缚的P‑C键，成功的解决了磷手性中心易于消旋化的科学难题，此类磷手性催化剂能够广泛的应用到手性膦催化的不对称环化等不对称反应中，具有广阔的商业应用前景。
Description
技术领域
本发明涉及本发明属于有机化学合成领域，具体涉及一种在手性膦催化的不对称合成领域应用的1-磷杂降冰片烯类有机膦催化剂、其合成方法及应用。
背景技术
在不对称催化领域，手性有机膦化物是重要有机催化剂。由于拥有一对孤对电子，三价磷化物可以直接作为亲核催化剂，进攻缺电子烯烃生成碳负离子中间体，进而催化化学反应。在手性膦催化剂的发展过程中，化学家往往把关注点放在了对于手性骨架的选择上，对于具有磷手性中心亲核膦催化剂的合成关注较少。磷本身的性质导致了磷手性中心难以合成而且高温下易于外消旋化，所以造成磷手性中心配体的研究非常少。然而有机膦小分子催化反应中反应的活性和对映选择性往往依赖于有机膦催化剂的电性、酸碱性和位阻，因此有机催化剂的微小变化常常能够影响催化反应的决速步骤。磷手性中心催化剂可以通过改变磷原子上取代基来改变催化剂的电子效应和位阻。并且这类催化剂的手性位点直接与反应底物相连，这就增加了手性诱导和传递的可能性。磷手性中心催化剂的这些优势促使化学家努力设计合成新型的磷手性催化剂，旨在克服制约其发展的其合成步骤繁琐且易于消旋的缺点，设计合成新型的磷手性催化剂。因为磷本身的性质导致了磷手性中心难以合成而且高温下易于外消旋化，所以造成磷手性中心配体的研究非常少。
到目前为止，将磷原子嵌入到刚性骨架中设计出具有磷手性中心手性有机膦催化剂仍然未见报道。
发明内容
针对目前的技术现状，本发明的目的之一在于提供一种1-磷杂降冰片烯类手性膦催化剂。其结构如下式III和III’所示：
式中，Ar为苯基、取代苯基、萘基、取代萘基；优选的，Ar为苯基、单取代苯基、萘基；更优选的，Ar为苯基、4-单取代苯基、2-萘基；更进一步优选的，Ar为苯基、4-甲基苯基、4-甲氧基苯基、4-苄基苯基、4-叔丁基苯基、4-叔丁氧基苯基苯基、2-萘基。
作为本发明的优选方案，所述1-磷杂降冰片烯类手性膦催化剂的结构如下所示：
本发明的目的之二在于提供所述催化剂的合成方法，所述方法以磷杂环戊二烯类化合物为中间产物，通过H[1,5]迁移和磷杂D-A反应生成1-磷杂降冰片烯类手性膦催化剂；所述反应式如下所示：
式中，Ar为苯基、取代苯基、萘基、取代萘基；优选的，Ar为苯基、单取代苯基、萘基；更优选的，Ar为苯基、4-单取代苯基、2-萘基；更进一步优选的，Ar为苯基、4-甲基苯基、4-甲氧基苯基、4-苄基苯基、4-叔丁基苯基、4-叔丁氧基苯基苯基、2-萘基。
作为本发明的优选方案，所述反应包括如下步骤：
步骤一)分别取I化合物原料于一定容积的Schlenk瓶中，惰性气体氛围下加入无水有机溶剂，低温下加入芳基格氏试剂，然后在此温度下继续反应至反应完全，淬灭反应，得到相应的产物II-a～II’-g；反应式如下：
步骤二)使用一定容积的Schlenk瓶，惰性气体氛围下，加入加氢试剂，洗涤；然后加入II化合物原料的无水四氢呋喃溶液；搅拌至反应完全，得到III-a～III’-g；其反应式如下所示：
作为本发明的优选方案，所述反应包括如下步骤：
步骤一)分别取I化合物原料于Schlenk瓶中，抽真空，充入氮气三次，加入无水四氢呋喃，在-78℃的条件下缓慢加入2.0当量的芳基格式试剂，然后在此温度下继续反应10h。TLC检测反应进程，当反应完全，向反应体系加入NH4Cl溶液，然后使用乙酸乙酯萃取，合并有机层，使用MgSO4干燥，过滤，减压蒸去溶剂，柱层析分离；得到相应的产物II-a～II’-g，产率39-46％；
步骤二)使用50mL的Schlenk瓶，抽真空，充入氮气三次，加入兰尼镍，使用无水乙醇洗涤三次，然后使用无水四氢呋喃洗涤三次。最后加入II化合物原料的无水四氢呋喃溶液；搅拌5小时，TLC检测反应，当反应完全，柱层析分离得到III-a～III’-g，产率71-87％。
本发明的另一目的在于提供了所述催化剂及其中间体的应用。具体是，以烯基羟吲哚衍生物作为缺电子的烯烃，实现了有机膦的基于取代的联烯酸酯的(4+2)环加成反应。优选的，所述催化剂为II-d；其反应式如下所示：
本发明还有一目的在于提供一种螺环化合物P1，所述螺环化合物P1结构如下，
优选的，所述化合物的非对映选择性大于20:1和/或立体选择性大于99％。
本发明提供选用烯基羟吲哚衍生物作为缺电子的烯烃，实现了有机膦催化的基于取代的联烯酸酯的(4+2)环加成反应。克服了使用传统的手性有机催化剂时，高温下无法实现有效的立体诱导的缺陷。
本发明实验过程中，通过对催化剂，溶剂，催化剂的当量和反应温度等条件的优化，发现使用II-d作为配体时效果最好(化合物II-d的X-ray X-ray crystal structure如附图1所示)。通过对反应底物上各个位置取代基的改变，进一步研究此类反应的底物适用性，能够以很高的产率(99％以上)，非对映选择性(大于20:1)以及立体选择性(大于99％)得到相应的螺环化合物P1，其结构如下，(化合物P1的X-ray X-ray crystal structure如附图2所示)。
有益效果：
1、本发明提供的催化剂作为一类结构新颖的手性膦催化剂，通过刚性骨架的引入，形成三个完全束缚的P-C键，成功的解决了磷手性中心易于消旋化的科学难题，此类磷手性催化剂能够广泛的应用到手性膦催化的不对称环化等不对称反应中，具有广阔的商业应用前景。2、本发明提供的合成方法简单、可行性好，收率较高。
附图说明
附图1：化合物II-d的X-ray X-ray crystal structure图；
附图2：螺环产物P1化合物P1的X-ray X-ray crystal structure图。
具体实施方式
为对本发明进行更好地说明，举实施例下：以下所用原料均为市售品。
实施例1化合物I的合成方法，步骤如下：
在N2环境下，将40mL甲醇，肉桂醛(20mmol),原甲酸三甲酯(40mmol)加入100mLSchlenk瓶中，然后加入催化剂对甲苯磺酸(10 mol％)，转入65℃油浴回流10h。反应完全后，加入少量NaOH固体，继续搅拌30 min。蒸去溶剂，过中性氧化铝干柱，旋干后得化合物A2，产率89％。
在N2环境下，将5mL甲苯，化合物A2(5.6mol)，phoshole(5.3mmol)加入75mLSchlenk瓶中。140℃油浴中反应2h。然后加入两当量的硫粉，过中性氧化铝柱(PE:DCM＝10:1)，得到化合物，产率52％。
在N2环境下，将20mL二氯甲烷，上步所得的化合物(10mmol)，三氟乙酸(20mmol)加入100mL Schlenk瓶中，室温搅拌3h。反应完全后用H2O洗涤(20mL*3)，MgSO4干燥。蒸干溶剂得化合物A4，产率94％。
White solid.31P NMR(121MHz,CDCl3)δ55.74(s)ppm.1H NMR(300MHz,CDCl3)δ1.41(s,3H,CH3),1.48(d,J＝2.6Hz,3H,CH3),2.14–2.29(m,2H,CH2),3.80–3.87(m,1H,CH),3.94(d,J＝5.8Hz,1H,CH),7.08–7.11(m,2H,CH),7.28–7.32(m,3H,CH),7.40–7.44(m,1H,CH),7.50–7.52(m,4H,CH),10.07(d,J＝1.4Hz,1H,CHO)ppm.13C NMR(75MHz,CDCl3)δ16.3(d,J＝12.8Hz,CH3),19.6(d,J＝17.3Hz,CH3),50.3(d,J＝19.5Hz,C),51.6(s,CH),52.4(d,J＝57.0Hz,CH2),58.3(d,J＝30.0Hz,CH),127.8(s,CH),128.1(d,J＝1.5Hz,CH),128.2(s,2CH),128.5(s,2CH),128.6(s,2CH),129.3(d,J＝6.0Hz,2CH),131.7(d,J＝10.5Hz,C),133.9(d,J＝67.5Hz,C),137.6(d,J＝6.0Hz,C),157.7(d,J＝15.0Hz,C),198.9(s,CHO)ppm.
在N2环境下，将40mLTHF，化合物A4(7.4mmol)，R-叔丁基磺酸亚胺(8mmol)，四异丙氧基钛(16mmol)加入100mL Schlenk瓶中，在50℃的条件下，油浴反应3h。用乙酸乙酯萃取(100mL*3)，MgSO4干燥。柱层析法分离(DCM：EA＝1:1)。得化合物I，产率80％。
Yellow solid.31P NMR(121MHz,CDCl3)δ57.68(s)ppm.1H NMR(300MHz,CDCl3)δ1.23(d,J＝13.3Hz,9H,3CH3),1.39(s,3H,CH3),1.53(dd,J＝4.3,2.6Hz,3H,CH3),2.24–2.39(m,2H,CH2),3.68–3.87(m,2H,CH),7.08–7.12(m,2H,CH),7.28–7.31(m,3H,CH),7.36–7.43(m,1H,CH),7.49–7.50(m,4H,CH),8.23–8.34(m,1H,CH)ppm.13C NMR(75MHz,CDCl3)δ16.3(d,J＝12.0Hz,CH3),19.8(d,J＝17.3Hz,CH3),22.7(d,J＝17.3Hz,3CH3),50.6(dd,J＝19.5,10.5Hz,C),52.8(dd,J＝61.5,35.3Hz,CH),52.8(dd,J＝55.5,11.3Hz,CH2),56.3(d,J＝9.0Hz,CH),57.5(dd,J＝28.5,2.3Hz,C),127.8(d,J＝3.0Hz,CH),128.0(s,,CH),128.3(d,J＝1.5Hz,2CH),128.5(d,J＝2.3Hz,2CH),128.5(s,2CH),129.3(dd,J＝5.3,1.5Hz,2CH),131.9(dd,J＝10.5,2.3Hz,C),134.6(dd,J＝68.3,9.0Hz,C),137.4–137.6(m,C),156.7(dd,J＝14.3,9.0Hz,C),165.8–166.6(m,CH)ppm.
实施例2化合物II-a至II’-g的合成方法，步骤如下：
分别取I化合物原料于50mL Schlenk瓶中，抽真空，充入氮气三次，加入无水四氢呋喃，在-78℃的条件下加入2.0当量的芳基格式试剂，然后再此温度下继续反应10h，当反应完全，向反应体系加入NH4Cl溶液，然后使用乙酸乙酯萃取，合并有机层，使用MgSO4干燥，过滤，减压蒸去溶剂，柱层析分离。得到相应的产物II-a～II’-g。产率：39-46％
代表性核磁数据II-e和II’-e:
II-d:White solid.31P NMR(121MHz,CDCl3)δ53.39(s)ppm.1H NMR(300MHz,CDCl3)δ1.11(s,3H,CH3),1.27(s,9H,3CH3),1.29(s,9H,3CH3),1.48(d,J＝2.4Hz,3H,CH3),1.54–1.60(m,1H,CH2),1.98(t,J＝10.3Hz,1H,CH2),2.95(d,J＝7.1Hz,1H,CH),3.00–3.08(m,1H,CH),4.76(ddd,J＝21.9,11.7,4.5Hz,1H,CH),5.88(d,J＝9.1Hz,1H,NH),7.01–7.04(m,2H,CH),7.24–7.27(m,3H,CH),7.33–7.35(m,2H,CH),7.38–7.51(m,5H,CH),7.57(d,J＝8.2Hz,2H,CH)ppm.13C NMR(75MHz,CDCl3)δ16.3(d,J＝12.0Hz,CH3),19.8(d,J＝16.5Hz,CH3),22.9(s,3CH3),31.3(s,3CH3),34.5(s,C),50.3(d,J＝18.8Hz,C),52.1(d,J＝26.3Hz,CH),52.7(d,J＝37.5Hz,CH2),54.3(d,J＝2.3Hz,CH),56.7(s,C),61.3(d,J＝3.0Hz,CH),125.3(s,2CH),127.6(s,CH),127.8(s,CH),128.4(s,2CH),128.5(s,6CH),129.1(d,J＝6.0Hz,2CH),132.4(d,J＝10.5Hz,C),135.9(d,J＝69.8Hz,C),136.1(d,J＝4.5Hz,C),137.7(d,J＝9.8Hz,C),150.7(s,C),155.9(d,J＝13.5Hz,C)ppm.
II’-d:White solid.31P NMR(121MHz,CDCl3)δ52.90(s)ppm.1H NMR(300MHz,CDCl3)δ1.09(s,3H,CH3),1.26(s,9H,3CH3),1.32–1.39(m,1H,CH2),1.34(s,9H,3CH3),1.44(d,J＝2.5Hz,3H,CH3),1.90–1.98(m,1H,CH2),2.90(d,J＝7.2Hz,1H,CH),3.53–3.60(m,1H,CH),4.79(ddd,J＝23.6,11.3,5.2Hz,1H,CH),6.34(d,J＝8.7Hz,1H,NH),7.06–7.09(m,2H,CH),7.22–7.30(m,3H,CH),7.33–7.39(m,1H,CH),7.41(d,J＝8.3Hz,2H,CH),7.47–7.49(m,4H,CH),7.61(d,J＝8.3Hz,2H,CH)ppm.13C NMR(75MHz,CDCl3)δ16.3(d,J＝12.0Hz,CH3),19.9(d,J＝16.5Hz,CH3),23.1(s,3CH3),31.4(s,3CH3),34.6(s,C),50.3(d,J＝19.5Hz,C),51.7(d,J＝42.0Hz,CH),52.4(d,J＝53.3Hz,CH2),55.2(d,J＝4.5Hz,CH),56.2(s,C),61.6(d,J＝3.8Hz,CH),125.1(s,2CH),127.6(s,CH),127.7(s,CH),128.5(s,4CH),128.6(s,2CH),128.9(s,2CH),129.3(d,J＝6.0Hz,2CH),132.3(d,J＝9.8Hz,C),136.0(d,J＝3.8Hz,C),137.0(s,C)137.3(d,J＝9.0Hz,C),150.8(s,C),155.5(d,J＝13.5Hz,C)ppm.
使用50mL的Schlenk瓶，抽真空，充入氮气三次，加入兰尼镍，使用无水乙醇洗涤三次，然后使用无水四氢呋喃洗涤三次。最后加入II化合物原料的无水四氢呋喃溶液。搅拌5小时，TLC检测反应，当反应完全，柱层析分离得到III-a～III’-g。产率：71-87％
代表性核磁数据：
(R)-N-((1R)-((1R,2R,4S)-4,5-dimethyl-3,6-diphenyl-1-phosphabicyclo[2.2.1]hept-5-en-2-yl)(phenyl)methyl)-2-methylpropane-2-sulfinamide III-a.
White solid.MP:145-146℃.[α]D＝-194(c＝0.1,CH2Cl2,19℃).31P NMR(121MHz,CDCl3)δ-20.06(s)ppm.1H NMR(300MHz,CDCl3)δ0.80–0.87(m,1H,CH2),1.13(s,9H,3CH3),1.42–1.47(m,1H,CH2),1.47(s,3H,CH3),2.69(d,J＝7.2Hz,1H,CH),2.78(t,J＝6.8Hz,1H,CH),3.64(d,J＝4.8Hz,1H,NH),4.53–4.60(m,1H,CH),7.08–7.11(m,2H,CH),7.23–7.46(m,13H,CH)ppm.13C NMR(75MHz,CDCl3)δ16.4(s,CH3),20.7(s,CH3),22.6(s,3CH3),48.0(d,J＝4.5Hz,CH2),54.7(d,J＝18.7Hz,CH),55.0(d,J＝2.3Hz,CH),56.2(s,C),61.6(d,J＝12.0Hz,CH),64.4(d,J＝5.3Hz,C),126.4(s,CH),126.9(s,CH),128.0(s,CH),128.1(s,CH),128.1(s,3CH),128.2(s,2CH),128.4(s,CH),128.5(s,CH),128.6(s,2CH),128.8(s,2CH),138.6(d,J＝21.0Hz,C),141.0(s,C),141.1(d,J＝1.5Hz,C),141.6(d,J＝21.0Hz,C),153.0(s,C)ppm.HRMS(ESI)m/z:[M+H]+calcd for C31H37NOPS 502.2328；Found502.2307.
(R)-N-((1S)-((1S,3S,4R)-4,5-dimethyl-3,6-diphenyl-1-phosphabicyclo[2.2.1]hept-5-en-2-yl)(phenyl)methyl)-2-methylpropane-2-sulfinamide III'-a.
White solid.MP:162-163℃.[α]D＝43(c＝0.1,CH2Cl2,24℃).31P NMR(121MHz,CDCl3)δ-18.63(s)ppm.1H NMR(300MHz,CDCl3)δ0.88(s,9H,3CH3),1.27(s,3H,CH3),1.49(s,3H,CH3),1.50–1.62(m,2H,CH2),2.63(dd,J＝10.2,6.5Hz,1H,CH),2.89(d,J＝6.4Hz,1H,CH),3.65(s,1H,NH),4.55(dd,J＝10.2,4.4Hz,1H,CH),7.2–7.4(m,15H,CH)ppm.13C NMR(75MHz,CDCl3)δ16.4(s,CH3),20.6(s,CH3),22.3(s,3CH3),48.2(d,J＝5.3Hz,CH2),55.3(s,C),56.3(d,J＝18.0Hz,CH),57.9(d,J＝2.3Hz,CH),64.3(d,J＝17.3Hz,CH),65.5(d,J＝5.3Hz,C),126.4(s,CH),127.2(s,CH),128.0(s,CH),128.2(s,CH),128.3(s,3CH),128.4(s,CH),128.4(s,3CH),128.4(s,2CH),129.2(s,2CH),138.5(d,J＝21.0Hz,C),141.2(s,C),141.7(d,J＝2.3Hz,C),141.9(s,C),152.7(s,C)ppm.HRMS(ESI)m/z:[M+H]+calcd forC31H37NOPS 502.2328；Found 502.2289.
(R)-N-((1R)-((1R,2R,4S)-4,5-dimethyl-3,6-diphenyl-1-phosphabicyclo[2.2.1]hept-5-en-2-yl)(p-tolyl)methyl)-2-methylpropane-2-sulfinamide III-b.
White solid.MP:179-180℃.[α]D＝-155(c＝0.1,CH2Cl2,18℃).31P NMR(121MHz,CDCl3)δ-20.39(s)ppm.1H NMR(300MHz,CDCl3)δ0.84–0.91(m,1H,CH2),1.12(s,9H,3CH3),1.15–1.16(m,3H,CH3),1.43–1.48(m,1H,CH2),1.48(s,3H,CH3),2.38(s,3H,CH3),2.70(d,J＝7.2Hz,1H,CH),2.78(t,J＝6.8Hz,1H,CH),3.59(d,J＝4.8Hz,1H,NH),4.49–4.57(m,1H,CH),7.09–7.15(m,2H,CH),7.17–7.39(m,12H,CH)ppm.13C NMR(75MHz,CDCl3)δ16.4(s,CH3),20.7(s,CH3),21.3(s,CH3),22.6(s,3CH3),48.1(d,J＝5.3Hz,CH2),54.7(d,J＝18.8Hz,CH),55.2(d,J＝2.3Hz,CH),56.1(s,C),61.5(d,J＝12.0Hz,CH),64.4(d,J＝12.8Hz,C),126.4(s,CH),126.8(s,CH),127.9(d,J＝4.5Hz,2CH),128.1(s,2CH),128.2(s,2CH),128.4(s,CH),128.5(s,CH),128.8(s,2CH),129.3(s,2CH),137.8(s,C),138.1(d,J＝2.3Hz,C),138.6(d,J＝20.3Hz,C),141.1(s,C),141.7(d,J＝15.8Hz,C),153.0(s,C)ppm.HRMS(ESI)m/z:[M+Na]+calcd for C32H38NOPSNa 538.2304；Found 538.2294.
(R)-N-((1S)-((1S,3S,4R)-4,5-dimethyl-3,6-diphenyl-1-phosphabicyclo[2.2.1]hept-5-en-2-yl)(p-tolyl)methyl)-2-methylpropane-2-sulfinamide III'-b.
White solid.MP:176-177℃.[α]D＝35(c＝0.1,CH2Cl2,26℃).31P NMR(121MHz,CDCl3)δ-18.59(s)ppm.1H NMR(300MHz,CDCl3)δ0.89(s,9H,3CH3),1.28(s,3H,CH3),1.49(s,3H,CH3),1.55–1.62(m,2H,CH2),2.37(s,3H,CH3),2.54(dd,J＝10.2,6.5Hz,1H,CH),2.90(d,J＝6.4Hz,1H,CH),3.67(s,1H,NH),4.53(dd,J＝10.3,4.4Hz,1H,CH),7.18–7.37(m,14H,CH)ppm.13C NMR(75MHz,CDCl3)δ16.4(s,CH3),20.6(s,CH3),21.4(s,CH3),22.3(s,3CH3),48.2(d,J＝6.0Hz,CH2),55.3(s,C),56.4(d,J＝17.3Hz,CH),57.9(d,J＝2.3Hz,CH),64.1(d,J＝17.3Hz,CH),65.5(d,J＝5.3Hz,C),126.4(s,CH),127.2(s,CH),128.2(s,CH),128.2(s,CH),128.3(s,4CH),128.4(s,2CH),129.2(s,4CH),137.6(s,C),138.6(d,J＝21.7Hz,C),138.6(d,J＝3.0Hz,C),141.3(s,C),141.9(d,J＝17.3Hz,C),152.7(s,C)ppm.HRMS(ESI)m/z:[M+Na]+calcd for C32H38NOPSNa 538.2304；Found 538.2291.
(R)-N-((1R)-[1,1'-biphenyl]-4-yl((1R,2R,4S)-4,5-dimethyl-3,6-diphenyl-1-phosphabicyclo[2.2.1]hept-5-en-2-yl)methyl)-2-methylpropane-2-sulfinamide III-c.
White solid.MP:82-83℃.[α]D＝-155(c＝0.1,CH2Cl2,20℃).31P NMR(121MHz,CDCl3)δ-19.61(s)ppm.1H NMR(300MHz,CDCl3)0.94–1.01(m,1H,CH2),1.16(s,9H,3CH3),1.17(s,3H,CH3),1.48–1.54(m,1H,CH2),1.50(s,3H,CH3),2.75(d,J＝7.2Hz,1H,CH),2.83(t,J＝6.9Hz,1H,CH),3.69(d,J＝5.2Hz,1H,NH),4.60–4.67(m,1H,CH),7.11–7.14(m,2H,CH),7.25–7.32(m,4H,CH),7.36–7.41(m,5H,CH),7.45–7.53(m,4H,CH),7.63–7.66(m,4H,CH)ppm.13C NMR(75MHz,CDCl3)δ16.4(s,CH3),20.7(s,CH3),22.6(s,3CH3),48.2(d,J＝4.5Hz,CH2),54.8(d,J＝18.7Hz,CH),55.2(d,J＝1.5Hz,CH),56.3(s,C),61.6(d,J＝12.0Hz,CH),64.5(d,J＝5.3Hz,C),126.4(s,CH),126.9(s,CH),127.1(s,2CH),127.2(s,2CH),127.4(s,CH),128.2(s,2CH),128.3(s,2CH),128.4(s,2CH),128.5(s,CH),128.5(s,CH),128.8(s,2CH),128.8(s,2CH),138.6(d,J＝21.0Hz,C),140.2(d,J＝2.3Hz,C),140.6(s,C),140.8(s,C),141.0(s,C),141.7(d,J＝15.8Hz,C),153.1(s,C)ppm.HRMS(ESI)m/z:[M+H]+calcd for C37H41NOPS 578.2641；Found 578.2651.
(R)-N-((1S)-[1,1'-biphenyl]-4-yl((1S,3S,4R)-4,5-dimethyl-3,6-diphenyl-1-phosphabicyclo[2.2.1]hept-5-en-2-yl)methyl)-2-methylpropane-2-sulfinamide III'-c.
White solid.MP:186-187℃.[α]D＝38(c＝0.1,CH2Cl2,26℃).31P NMR(121MHz,CDCl3)δ-18.76(s)ppm.1H NMR(300MHz,CDCl3)δ0.90(s,9H,3CH3),1.29(s,3H,CH3),1.50(s,3H,CH3),1.58–1.68(m,2H,CH2),2.56(dd,J＝10.2,6.4Hz,1H,CH),2.92(d,J＝6.4Hz,1H,CH),3.69(s,1H,NH),4.60(dd,J＝10.3,4.6Hz,1H,CH),7.18–7.37(m,11H,CH),7.43–7.48(m,4H,CH),7.61–7.67(m,4H,CH)ppm.13C NMR(75MHz,CDCl3)δ16.4(s,CH3),20.6(s,CH3),22.3(s,3CH3),48.2(d,J＝5.3Hz,CH2),55.4(s,C),56.2(d,J＝18.0Hz,CH),57.9(s,CH),64.0(d,J＝17.3Hz,CH),65.5(d,J＝4.5Hz,C),126.4(s,CH),127.0(s,2CH),127.1(s,2CH),127.2(s,CH),127.3(s,CH),128.2(s,CH),128.3(s,3CH),128.4(s,2CH),128.7(s,2CH),128.8(s,CH),128.8(s,CH),129.2(s,2CH),138.5(d,J＝21.0Hz,C),140.6(s,C),140.7(s,C),140.8(s,C),141.2(s,C),141.8(d,J＝16.5Hz,C),152.8(s,C)ppm.HRMS(ESI)m/z:[M+H]+calcd for C37H41NOPS 578.2641；Found 578.2635.
(R)-N-((1R)-(4-(tert-butyl)phenyl)((1R,2R,4S)-4,5-dimethyl-3,6-diphenyl-1-phosphabicyclo[2.2.1]hept-5-en-2-yl)methyl)-2-methylpropane-2-sulfinamide III-d.
White solid.MP:164-165℃.[α]D＝-216(c＝0.1,CH2Cl2,21℃).31P NMR(121MHz,CDCl3)δ-21.49(s)ppm.1H NMR(300MHz,CDCl3)δ0.80(t,J＝21.4Hz,1H,CH2),1.14(s,3H,CH3),1.16(s,9H,3CH3),1.35(s,9H,3CH3),1.44–1.50(m,1H,CH2),1.49(s,3H,CH3),2.68(d,J＝7.3Hz,1H,CH),2.81(t,J＝6.6Hz,1H,CH),3.66(d,J＝4.4Hz,1H,NH),4.57–4.64(m,1H,CH),7.10(d,J＝6.7Hz,2H,CH),7.23–7.27(m,4H,CH),7.38–7.42(m,8H,CH)ppm.13C NMR(75MHz,CDCl3)δ16.4(s,CH3),20.8(s,CH3),22.6(s,3CH3),31.4(s,3CH3),34.6(s,C),48.1(d,J＝4.5Hz,CH2),54.5(s,CH),54.8(s,CH),56.2(s,C),61.0(d,J＝10.5Hz,CH),64.3(d,J＝42.8Hz,C),125.4(s,2CH),126.4(s,CH),126.8(s,CH),127.7(d,J＝3.8Hz,2CH),128.1(s,2CH),128.2(s,2CH),128.5(d,J＝7.5Hz,2CH),128.8(s,2CH),137.9(d,J＝1.5Hz,C),138.7(d,J＝21.0Hz,C),141.0(s,C),141.8(d,J＝15.8Hz,C),151.0(s,C),152.9(s,C)ppm.HRMS(ESI)m/z:[M+H]+calcd for C35H45NOPS 558.2954；Found 558.2956.
N-((1S)-(4-(tert-butyl)phenyl)((1S,3S,4R)-4,5-dimethyl-3,6-diphenyl-1-sulfido-1-phosphabicyclo[2.2.1]hept-5-en-2-yl)methyl)-2-methylpropane-2-sulfinamide III'-d.
White solid.MP:169-170℃.[α]D＝10(c＝0.1,CH2Cl2,25℃).31P NMR(121MHz,CDCl3)δ-18.08(s)ppm.1H NMR(300MHz,CDCl3)δ0.91(s,9H,3CH3),1.27(s,3H,CH3),1.35(s,9H,3CH3),1.49(s,3H,CH3),1.54–1.64(m,2H,CH2),2.51–2.56(m,1H,CH),2.90(d,J＝6.4Hz,1H,CH),3.65(s,1H,NH),4.55(dd,J＝9.7,5.0Hz,1H,CH),7.17–7.40(m,14H,CH)ppm.13C NMR(75MHz,CDCl3)δ16.4(s,CH3),20.6(s,CH3),22.4(s,3CH3),31.5(s,3CH3),34.6(s,C),48.2(d,J＝4.5Hz,CH2),55.3(s,C),56.4(d,J＝17.3Hz,CH),57.6(d,J＝2.3Hz,CH),63.6(d,J＝17.3Hz,CH),65.4(d,J＝5.3Hz,C),125.2(s,2CH),126.4(s,CH),127.1(s,CH),128.0(d,J＝3.0Hz,2CH),128.2–128.3(m,4CH),128.4(s,2CH),129.2(s,2CH),138.4(d,J＝3.0Hz,C),138.7(s,C),141.2(s,C),141.9(d,J＝16.5Hz,C)150.7(s,C),152.7(s,C)ppm.HRMS(ESI)m/z:[M+H]+calcd for C35H45NOPS 558.2954；Found 558.2952.
(1R)-(4-(tert-butyl)phenyl)((1R,2R,4S)-4,5-dimethyl-3,6-diphenyl-1-phosphabicyclo[2.2.1]hept-5-en-2-yl)methanamine 5e.
White solid.MP:54-55℃.[α]D＝-189(c＝0.1,CH2Cl2,21℃).31P NMR(121MHz,CDCl3)δ-20.83(s)ppm.1H NMR(300 MHz,CDCl3)δ1.06(t,J＝10.6Hz,1H,CH2),1.17(s,3H,CH3),1.32(s,9H,3CH3),1.47–1.53(m,1H,CH2),1.50(s,3H,CH3),1.76(s,2H,NH2),2.56(t,J＝6.3Hz,1H,CH),2.77(d,J＝6.8Hz,1H,CH),4.21–4.26(m,1H,CH),7.05(d,J＝7.0Hz,2H,CH),7.17–7.31(m,8H,CH),7.40–7.41(m,4H,CH)ppm.13C NMR(75MHz,CDCl3)δ16.4(s,CH3),20.7(s,CH3),31.4(s,3CH3),34.4(s,C),48.5(d,J＝3.0Hz,CH2),54.9(d,J＝2.3Hz,CH),56.2(d,J＝17.3Hz,CH),58.3(d,J＝12.0Hz,CH),64.3(d,J＝4.5Hz,C),125.0(s,2CH),126.3(s,2CH),126.8(d,J＝3.0Hz,2CH),127.8(s,2CH),128.3(s,2CH),128.5(s,CH),128.6(s,CH),128.8(s,2CH)138.8(d,J＝21.0Hz,C),141.5(d,J＝3.0Hz,C),141.8(s,C),142.0(s,C),149.9(s,C),153.0(s,C)ppm.HRMS(ESI)m/z:[M+Na]+calcd for C31H36NPNa476.2478；Found 476.2430.
最后说明的是，以上实施例仅用以说明本发明的技术方案而非限制，本领域普通技术人员对本发明的技术方案所做的其他修改或者等同替换，只要不脱离本发明技术方案的精神和范围，均应涵盖在本发明的权利要求范围当中。
Claims (5)
1.一种1-磷杂降冰片烯类手性膦催化剂，其特征在于，结构如下式III和III’所示：
式中，Ar为苯基、4-甲基苯基、4-苯基苯基、4-正丁基苯基、4-叔丁基苯基、4-叔丁氧基苯基或2-萘基。
2.一种1-磷杂降冰片烯类手性膦催化剂，其特征在于，所述催化剂的结构如下所示：
3.根据权利要求2所述催化剂的合成方法，其特征在于，所述方法以式Ⅰ化合物为中间产物，通过H[1,5]迁移和磷杂D-A反应生成1-磷杂降冰片烯类手性膦催化剂；所述反应式如下所示：
III和III’的结构式如III-a～III’-g所示。
4.根据权利要求3所述的合成方法，其特征在于，所述反应包括如下步骤：
步骤一)分别取I化合物原料于一定容积的Schlenk瓶中，惰性气体氛围下加入无水有机溶剂，低温下加入芳基格氏试剂，然后在此温度下继续反应至反应完全，淬灭反应，得到相应的产物II-a～II’-g；反应式如下：
步骤二)使用一定容积的Schlenk瓶，惰性气体氛围下，加入Raney Ni，洗涤；然后加入II化合物原料的无水四氢呋喃溶液；搅拌至反应完全，得到III-a～III’-g；其反应式如下所示：
5.根据权利要求3或4所述的合成方法，其特征在于，所述反应包括如下步骤：
步骤一)分别取I化合物原料于Schlenk瓶中，抽真空，充入氮气三次，加入无水四氢呋喃，在-78℃的条件下缓慢加入2.0当量的芳基格式试剂，然后在此温度下继续反应10h，TLC检测反应进程，当反应完全，向反应体系加入NH4Cl溶液，然后使用乙酸乙酯萃取，合并有机层，使用MgSO4干燥，过滤，减压蒸去溶剂，柱层析分离；得到相应的产物II-a～II’-g，产率39-46％；
步骤二)使用50mL的Schlenk瓶，抽真空，充入氮气三次，加入兰尼镍，使用无水乙醇洗涤三次，然后使用无水四氢呋喃洗涤三次；最后加入II化合物原料的无水四氢呋喃溶液；搅拌5小时，TLC检测反应，当反应完全，柱层析分离得到III-a～III’-g，产率71-87％。
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202110018741.2A CN112851710B (zh) | 2021-01-07 | 2021-01-07 | 1-磷杂降冰片烯类手性膦催化剂、其合成方法及应用 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202110018741.2A CN112851710B (zh) | 2021-01-07 | 2021-01-07 | 1-磷杂降冰片烯类手性膦催化剂、其合成方法及应用 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN112851710A CN112851710A (zh) | 2021-05-28 |
| CN112851710B true CN112851710B (zh) | 2022-08-23 |
Family
ID=76004866
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202110018741.2A Expired - Fee Related CN112851710B (zh) | 2021-01-07 | 2021-01-07 | 1-磷杂降冰片烯类手性膦催化剂、其合成方法及应用 |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN112851710B (zh) |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109232650A (zh) * | 2018-11-01 | 2019-01-18 | 郑州大学 | 手性1-磷杂降冰片二烯衍生物及其合成方法 |
| CN109503660A (zh) * | 2018-12-25 | 2019-03-22 | 华东师范大学 | 一类环状膦骨架的手性单膦催化剂Le-Phos及其全构型的制备方法和应用 |
-
2021
- 2021-01-07 CN CN202110018741.2A patent/CN112851710B/zh not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN109232650A (zh) * | 2018-11-01 | 2019-01-18 | 郑州大学 | 手性1-磷杂降冰片二烯衍生物及其合成方法 |
| CN109503660A (zh) * | 2018-12-25 | 2019-03-22 | 华东师范大学 | 一类环状膦骨架的手性单膦催化剂Le-Phos及其全构型的制备方法和应用 |
Non-Patent Citations (3)
| Title |
|---|
| Design of 1‑Phosphanorbornene Derivatives as Chiral Organocatalysts for Enantioselective (4 + 2) Annulation Reactions of γ‑Benzyl Allenoates;Siming Jia 等;《Org. Lett.》;20210414;第23卷;3337−3342 * |
| Qiu-Zhen Xi 等.Brønsted Acid Tuned, Lewis Base Promoted [4 + 2] Annulation Reactions of Allenoates with Electron‐Deficient Olefins.《Eur.J.Org.Chem.》.2018,4917-4925. * |
| Synthesis of 3,3’ -Spirocyclic Oxindoles via Phosphine Catalyzed [4 +2] Cyclizations;Maxime Gicquel等;《Org. Lett.》;20130723;第15卷(第15期);第4002-4005页 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN112851710A (zh) | 2021-05-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US6130340A (en) | Asymmetric cycloaddition reactions | |
| CA2082166C (en) | Chiral phospholane transition metal catalysts | |
| JP5685071B2 (ja) | 新規ルテニウム錯体及びこれを触媒とする光学活性アルコール化合物の製造方法 | |
| JP6391588B2 (ja) | 非対称不飽和ｎ‐ヘテロ環状ジアミノカルベンを含むルテニウム錯体 | |
| JP2011518788A (ja) | スピロホスフィン−オキサゾリン、その製造方法、及びその応用 | |
| CN110062655B (zh) | 有机金属络合物催化剂 | |
| US20140336402A1 (en) | Ligand forming asymmetrical transformation catalyst for making new pharmaceuticals | |
| CN104402718B (zh) | 一种手性烯丙酯类化合物及其制备方法 | |
| US20140187809A1 (en) | Novel ruthenium complex and process for producing optically active alcohol compound using same as catalyst | |
| CN112851710B (zh) | 1-磷杂降冰片烯类手性膦催化剂、其合成方法及应用 | |
| CN109232650B (zh) | 手性1-磷杂降冰片二烯衍生物及其合成方法 | |
| CN109503660B (zh) | 一类环状膦骨架的手性单膦催化剂Le-Phos及其全构型的制备方法和应用 | |
| JP4050294B2 (ja) | 光学活性コバルト（ｉｉ）錯体 | |
| US5322956A (en) | Chiral phospholane transition metal catalysts | |
| JP3040353B2 (ja) | ルテニウム−ジアミン錯体及びこれを触媒とする光学活性アルコール類の製造方法 | |
| US20090227805A1 (en) | Axially Asymmetric Phosphorus Compound and Production Method Thereof | |
| JP3957346B2 (ja) | 光学活性アルコールの製造方法 | |
| US20080139822A1 (en) | Novel optically active biaryl phosphorus compound and production process thereof | |
| CN108290910B (zh) | N,n-双(2-二烷基膦乙基)胺-硼烷配合物及其制造方法及以该胺为配体的钌配合物的制造方法 | |
| CN101835745B (zh) | 二磺酸化合物的制法、不对称曼尼希催化剂、β-氨基羰基衍生物的制法及二磺酸盐 | |
| CN106518931B (zh) | 一种新型螺环膦-羧酸的铱络合物及其制备方法和应用 | |
| CN115850328B (zh) | 环丙烷骨架双膦配体与其钴配合物和制备方法及应用 | |
| WO2022074177A1 (en) | Dynamic kinetic resolution of alcohols by enantioselective silylation | |
| CN115477672A (zh) | 一种含有轴手性和膦中心手性化合物及其制备方法 | |
| CN117567492A (zh) | 一种手性氮杂卡宾-硼烷及其在催化不对称环化异构化反应中的应用 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| GR01 | Patent grant | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20220823 |
|
| CF01 | Termination of patent right due to non-payment of annual fee |