CN105944676B - 一种呋喃二甲酸庚酯纯化用吸附剂的制备方法 - Google Patents
一种呋喃二甲酸庚酯纯化用吸附剂的制备方法 Download PDFInfo
- Publication number
- CN105944676B CN105944676B CN201610259814.6A CN201610259814A CN105944676B CN 105944676 B CN105944676 B CN 105944676B CN 201610259814 A CN201610259814 A CN 201610259814A CN 105944676 B CN105944676 B CN 105944676B
- Authority
- CN
- China
- Prior art keywords
- furandicarboxylic acid
- adsorbent
- heptyl ester
- acid heptyl
- product
- 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.)
- Active
Links
- VQVMNNDRPOUXMK-UHFFFAOYSA-N 2-heptoxycarbonylfuran-3-carboxylic acid Chemical compound CCCCCCCOC(=O)c1occc1C(O)=O VQVMNNDRPOUXMK-UHFFFAOYSA-N 0.000 title claims abstract description 20
- 239000003463 adsorbent Substances 0.000 title claims abstract description 17
- 238000002360 preparation method Methods 0.000 title claims abstract description 10
- KAESVJOAVNADME-UHFFFAOYSA-N 1H-pyrrole Natural products C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 8
- 125000004215 2,4-difluorophenyl group Chemical group [H]C1=C([H])C(*)=C(F)C([H])=C1F 0.000 claims description 8
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 claims description 8
- 239000013067 intermediate product Substances 0.000 claims description 8
- DLEDOFVPSDKWEF-UHFFFAOYSA-N lithium butane Chemical compound [Li+].CCC[CH2-] DLEDOFVPSDKWEF-UHFFFAOYSA-N 0.000 claims description 8
- MZRVEZGGRBJDDB-UHFFFAOYSA-N n-Butyllithium Substances [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 6
- 239000002808 molecular sieve Substances 0.000 claims description 6
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 claims description 6
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims description 6
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 5
- 238000010792 warming Methods 0.000 claims description 5
- 239000000047 product Substances 0.000 description 16
- HYBBIBNJHNGZAN-UHFFFAOYSA-N furfural Chemical compound O=CC1=CC=CO1 HYBBIBNJHNGZAN-UHFFFAOYSA-N 0.000 description 12
- -1 heptyl heptylate Chemical compound 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 238000000746 purification Methods 0.000 description 4
- NOEGNKMFWQHSLB-UHFFFAOYSA-N 5-hydroxymethylfurfural Chemical compound OCC1=CC=C(C=O)O1 NOEGNKMFWQHSLB-UHFFFAOYSA-N 0.000 description 3
- RJGBSYZFOCAGQY-UHFFFAOYSA-N hydroxymethylfurfural Natural products COC1=CC=C(C=O)O1 RJGBSYZFOCAGQY-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- GSNUFIFRDBKVIE-UHFFFAOYSA-N 2,5-dimethylfuran Chemical compound CC1=CC=C(C)O1 GSNUFIFRDBKVIE-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000013065 commercial product Substances 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- LJJVZJSGXHJIPP-UHFFFAOYSA-N ethylpentyl Chemical group [CH2+]CCC[CH]C[CH2-] LJJVZJSGXHJIPP-UHFFFAOYSA-N 0.000 description 2
- CHTHALBTIRVDBM-UHFFFAOYSA-N furan-2,5-dicarboxylic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)O1 CHTHALBTIRVDBM-UHFFFAOYSA-N 0.000 description 2
- 150000002240 furans Chemical class 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- SMNDYUVBFMFKNZ-UHFFFAOYSA-N 2-furoic acid Chemical class OC(=O)C1=CC=CO1 SMNDYUVBFMFKNZ-UHFFFAOYSA-N 0.000 description 1
- XGJWKRJQEOSFCO-UHFFFAOYSA-N 5-(chloromethyl)furan-2-carboxylic acid Chemical compound OC(=O)C1=CC=C(CCl)O1 XGJWKRJQEOSFCO-UHFFFAOYSA-N 0.000 description 1
- OVOCLWJUABOAPL-UHFFFAOYSA-N 5-methylfuran-2-carboxylic acid Chemical compound CC1=CC=C(C(O)=O)O1 OVOCLWJUABOAPL-UHFFFAOYSA-N 0.000 description 1
- CMJBUVNYQIMCQH-UHFFFAOYSA-N C(CCCC)OC(=O)C=1OC=CC1C(=O)O Chemical compound C(CCCC)OC(=O)C=1OC=CC1C(=O)O CMJBUVNYQIMCQH-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical group C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- SRKKQWSERFMTOX-UHFFFAOYSA-N cyclopentane;titanium Chemical compound [Ti].[CH]1C=CC=C1 SRKKQWSERFMTOX-UHFFFAOYSA-N 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- DNXDYHALMANNEJ-UHFFFAOYSA-N furan-2,3-dicarboxylic acid Chemical compound OC(=O)C=1C=COC=1C(O)=O DNXDYHALMANNEJ-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Classifications
-
- 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
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/22—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
-
- 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
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/22—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
- B01J20/223—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material containing metals, e.g. organo-metallic compounds, coordination complexes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- 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
- B01J2220/00—Aspects relating to sorbent materials
- B01J2220/40—Aspects relating to the composition of sorbent or filter aid materials
- B01J2220/44—Materials comprising a mixture of organic materials
-
- 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
- B01J2220/00—Aspects relating to sorbent materials
- B01J2220/50—Aspects relating to the use of sorbent or filter aid materials
- B01J2220/58—Use in a single column
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Analytical Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Pyrrole Compounds (AREA)
Abstract
Description
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610259814.6A CN105944676B (zh) | 2016-04-26 | 2016-04-26 | 一种呋喃二甲酸庚酯纯化用吸附剂的制备方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610259814.6A CN105944676B (zh) | 2016-04-26 | 2016-04-26 | 一种呋喃二甲酸庚酯纯化用吸附剂的制备方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN105944676A CN105944676A (zh) | 2016-09-21 |
CN105944676B true CN105944676B (zh) | 2019-02-19 |
Family
ID=56915846
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201610259814.6A Active CN105944676B (zh) | 2016-04-26 | 2016-04-26 | 一种呋喃二甲酸庚酯纯化用吸附剂的制备方法 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN105944676B (zh) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996031494A1 (en) * | 1995-04-05 | 1996-10-10 | Chronopol, Inc. | Method to produce and purify cyclic esters |
CN1332183A (zh) * | 2001-07-25 | 2002-01-23 | 巴陵石化岳阳石油化工总厂 | 一种由偶联法制备的含共轭二烯烃的苯乙烯类嵌段聚合物的选择氢化方法 |
CN103380121A (zh) * | 2011-02-24 | 2013-10-30 | 赢创奥克森诺有限责任公司 | 作为增塑剂的呋喃二甲酸庚酯 |
CN103380120A (zh) * | 2011-02-24 | 2013-10-30 | 赢创奥克森诺有限责任公司 | 作为增塑剂的呋喃二甲酸戊酯 |
CN103459431A (zh) * | 2011-05-27 | 2013-12-18 | 旭化成化学株式会社 | 氢化共轭二烯系共聚物的制造方法 |
-
2016
- 2016-04-26 CN CN201610259814.6A patent/CN105944676B/zh active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996031494A1 (en) * | 1995-04-05 | 1996-10-10 | Chronopol, Inc. | Method to produce and purify cyclic esters |
CN1332183A (zh) * | 2001-07-25 | 2002-01-23 | 巴陵石化岳阳石油化工总厂 | 一种由偶联法制备的含共轭二烯烃的苯乙烯类嵌段聚合物的选择氢化方法 |
CN103380121A (zh) * | 2011-02-24 | 2013-10-30 | 赢创奥克森诺有限责任公司 | 作为增塑剂的呋喃二甲酸庚酯 |
CN103380120A (zh) * | 2011-02-24 | 2013-10-30 | 赢创奥克森诺有限责任公司 | 作为增塑剂的呋喃二甲酸戊酯 |
CN103459431A (zh) * | 2011-05-27 | 2013-12-18 | 旭化成化学株式会社 | 氢化共轭二烯系共聚物的制造方法 |
Non-Patent Citations (1)
Title |
---|
活化条件对二氯二茂钛/正丁基锂催化苯乙烯-丁二烯-苯乙烯嵌段共聚物加氢反应的影响;张娜娜等;《合成橡胶工业》;20140315;第87-90页 |
Also Published As
Publication number | Publication date |
---|---|
CN105944676A (zh) | 2016-09-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN109384809B (zh) | 一种去除二甲基硅氧烷环体中线性硅氧烷的方法 | |
CN102260228A (zh) | 一步合成油酸山梨坦、司盘-80药用辅料的生产工艺 | |
CN103435484A (zh) | 高纯度甲基丙烯酸羟烷酯的制备工艺 | |
CN111499603B (zh) | 一种催化转化糠醛制备糠醇的方法 | |
CN105944676B (zh) | 一种呋喃二甲酸庚酯纯化用吸附剂的制备方法 | |
CN108640943B (zh) | 一种利用硅粉生产正硅酸乙酯的方法 | |
CN112321557B (zh) | 一种佳乐麝香的制备方法 | |
CN107413333B (zh) | 用于生产高纯度氯乙酸的改性加氢脱氯催化剂及制备方法 | |
CN101792426A (zh) | 乙基四氢糠基醚的合成方法 | |
CN112717988A (zh) | 一种高效无污染用于制备乙酰正丙醇的催化剂及其制备方法、使用方法 | |
CN105801474B (zh) | 一种精制3,6‑二氯吡啶甲酸的方法 | |
CN105906592B (zh) | 一种2-呋喃甲酸异戊酯纯化的方法 | |
CN104059097B (zh) | 一种歧化制备二甲基二氯硅烷的方法 | |
CN107312177A (zh) | 一种制切削液用聚醚改性硅油的制备方法 | |
CN110938207A (zh) | 一种含氢硅油的制备方法 | |
CN111135831A (zh) | 一种2-甲基呋喃气相加氢制2-甲基四氢呋喃催化剂的制备方法 | |
CN105732694A (zh) | 一种吸附提纯1,1,1,3,5,5,5-七甲基三硅氧烷的方法 | |
CN103819495A (zh) | 倍他米松中间体的制备方法 | |
CN104926599A (zh) | 一种在新型溶剂体系下制备高纯度联苯二氯苄的方法 | |
CN1271065C (zh) | α-生育酚的制备方法 | |
CN103709039A (zh) | Cu-丝光沸石催化合成没食子酸甲(乙)酯的方法 | |
CN103449954A (zh) | 高纯度长叶烯的制备方法 | |
CN105884721B (zh) | 一种2,5‑呋喃二甲醛纯化的方法 | |
CN105732551B (zh) | 一种提纯生物基2,5‑呋喃二甲酸的方法 | |
CN105777542A (zh) | 一种柠檬酸三乙酯纯化的方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
CB02 | Change of applicant information |
Address after: 432000 Hubei city of Xiaogan province high tech Zone Qun Sheng Cun Nan Qu Bian min Lu 5 floor, room 91 Applicant after: Zhang Ling Address before: 432000 Hubei city of Xiaogan province high tech Zone Danyang District Community Lisi mall two Room 201 Applicant before: Zhang Ling |
|
COR | Change of bibliographic data | ||
CB02 | Change of applicant information |
Address after: 432000, 11 business street, Danyang office, hi tech Zone, Hubei, Xiaogan Applicant after: Zhang Ling Address before: 432000 Hubei city of Xiaogan province high tech Zone Qun Sheng Cun Nan Qu Bian min Lu 5 floor, room 91 Applicant before: Zhang Ling |
|
CB02 | Change of applicant information | ||
CB02 | Change of applicant information | ||
CB02 | Change of applicant information |
Address after: Binwang zipper street 322000 Yiwu city in Zhejiang province Jinhua city 5 District No. 3 room 602 Applicant after: Zhang Ling Address before: 432000, 11 business street, Danyang office, hi tech Zone, Hubei, Xiaogan Applicant before: Zhang Ling |
|
GR01 | Patent grant | ||
GR01 | Patent grant | ||
TR01 | Transfer of patent right | ||
TR01 | Transfer of patent right |
Effective date of registration: 20220531 Address after: 475500 east section of Renmin Road, Kaifeng City, Henan Province (Jialu River Beach) Patentee after: HENAN KANGYUAN SPICE FACTORY Co.,Ltd. Address before: 322000 Room 602, No. 3, 5 District, Binwang Zipper Street, Yiwu City, Jinhua City, Zhejiang Province Patentee before: Zhang Ling |