JPS6233139A - ２−アミノベンジルアルコ−ル類の製造法 - Google Patents
２−アミノベンジルアルコ−ル類の製造法Info
- Publication number
- JPS6233139A JPS6233139A JP60171026A JP17102685A JPS6233139A JP S6233139 A JPS6233139 A JP S6233139A JP 60171026 A JP60171026 A JP 60171026A JP 17102685 A JP17102685 A JP 17102685A JP S6233139 A JPS6233139 A JP S6233139A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- zinc chloride
- added
- mol
- anthranilic acid
- 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.)
- Granted
Links
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- VYFOAVADNIHPTR-UHFFFAOYSA-N isatoic anhydride Chemical compound NC1=CC=CC=C1CO VYFOAVADNIHPTR-UHFFFAOYSA-N 0.000 title abstract description 7
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 claims abstract description 26
- 235000005074 zinc chloride Nutrition 0.000 claims abstract description 13
- 239000011592 zinc chloride Substances 0.000 claims abstract description 13
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 claims abstract description 8
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 5
- -1 2-aminobenzyl alcohols Chemical class 0.000 claims description 14
- 239000012279 sodium borohydride Substances 0.000 claims description 11
- 229910000033 sodium borohydride Inorganic materials 0.000 claims description 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 3
- 238000000034 method Methods 0.000 abstract description 9
- 239000003153 chemical reaction reagent Substances 0.000 abstract description 3
- 150000001875 compounds Chemical class 0.000 abstract description 3
- OOKMNUXTRORHIA-UHFFFAOYSA-N [2-(dimethylamino)phenyl]methanol Chemical compound CN(C)C1=CC=CC=C1CO OOKMNUXTRORHIA-UHFFFAOYSA-N 0.000 abstract description 2
- 239000003905 agrochemical Substances 0.000 abstract description 2
- 239000003814 drug Substances 0.000 abstract description 2
- 239000002994 raw material Substances 0.000 abstract description 2
- MOOAHMCRPCTRLV-UHFFFAOYSA-N boron sodium Chemical compound [B].[Na] MOOAHMCRPCTRLV-UHFFFAOYSA-N 0.000 abstract 3
- 229940079593 drug Drugs 0.000 abstract 1
- ZCNSBHAIPOWHJE-UHFFFAOYSA-N methyl 2-dimethylaminobenzoate Chemical compound COC(=O)C1=CC=CC=C1N(C)C ZCNSBHAIPOWHJE-UHFFFAOYSA-N 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 18
- 239000000243 solution Substances 0.000 description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- 238000001816 cooling Methods 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000002198 insoluble material Substances 0.000 description 4
- 239000012280 lithium aluminium hydride Substances 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 3
- 238000006722 reduction reaction Methods 0.000 description 3
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- WORJEOGGNQDSOE-UHFFFAOYSA-N chloroform;methanol Chemical compound OC.ClC(Cl)Cl WORJEOGGNQDSOE-UHFFFAOYSA-N 0.000 description 2
- 239000012230 colorless oil Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- GVOWHGSUZUUUDR-UHFFFAOYSA-N methyl N-methylanthranilate Chemical compound CNC1=CC=CC=C1C(=O)OC GVOWHGSUZUUUDR-UHFFFAOYSA-N 0.000 description 2
- 239000010446 mirabilite Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- INGIXPMMNAFVHF-UHFFFAOYSA-N 2-(1h-benzimidazol-2-ylsulfinylmethyl)aniline Chemical class NC1=CC=CC=C1CS(=O)C1=NC2=CC=CC=C2N1 INGIXPMMNAFVHF-UHFFFAOYSA-N 0.000 description 1
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 description 1
- 108010074725 Alpha,alpha-trehalose phosphorylase Proteins 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- 239000003699 antiulcer agent Substances 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 150000003938 benzyl alcohols Chemical class 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- WKRKXDRSJVDMGO-UHFFFAOYSA-N ethyl 2-(diethylamino)benzoate Chemical compound CCOC(=O)C1=CC=CC=C1N(CC)CC WKRKXDRSJVDMGO-UHFFFAOYSA-N 0.000 description 1
- 230000009931 harmful effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- RSIJVJUOQBWMIM-UHFFFAOYSA-L sodium sulfate decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[O-]S([O-])(=O)=O RSIJVJUOQBWMIM-UHFFFAOYSA-L 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60171026A JPS6233139A (ja) | 1985-08-05 | 1985-08-05 | ２−アミノベンジルアルコ−ル類の製造法 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60171026A JPS6233139A (ja) | 1985-08-05 | 1985-08-05 | ２−アミノベンジルアルコ−ル類の製造法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6233139A true JPS6233139A (ja) | 1987-02-13 |
| JPH0558420B2 JPH0558420B2 (cs) | 1993-08-26 |
Family
ID=15915708
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60171026A Granted JPS6233139A (ja) | 1985-08-05 | 1985-08-05 | ２−アミノベンジルアルコ−ル類の製造法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6233139A (cs) |
-
1985
- 1985-08-05 JP JP60171026A patent/JPS6233139A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0558420B2 (cs) | 1993-08-26 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3544590A (en) | Cyclic amines and the process for their formation | |
| EP0068407A1 (en) | Aminosulfonylbenzoic acid derivatives | |
| ES471960A1 (es) | Procedimiento para la preparacion de compuestos que contie- nen enlaces de fosforo-carbono-nitrogeno | |
| JPS6233139A (ja) | ２−アミノベンジルアルコ−ル類の製造法 | |
| DK0612310T3 (da) | Fremgangsmåde til fremstilling af kanelsyrederivater | |
| JPS6440467A (en) | Novel substituted diphenylimidazole derivative | |
| JPS5949221B2 (ja) | ３−アシルアミノ−４−ホモイソツイスタンの製造法 | |
| US3900476A (en) | 2(2'-pyrimidylamino)quinazolines and their preparation | |
| DeTar et al. | Intramolecular Reactions. IV. Chain Transfer Reaction Involving an Aromatic Hydrogen Atom and Related Reactions of 2-(4'-Methylbenzoyl)-benzenediazonium Salts1 | |
| Červinka et al. | Absolute configurations of some heterocyclic acids | |
| Forbes et al. | An Extension of the Woodward Rules Concerning Alkyl Substituents in Conjugated Aliphatic Systems | |
| JPS61229873A (ja) | ２‐メルカプトベンゾオキサゾールの製法 | |
| US3293260A (en) | 1-substituted cycloheptimidazol-2(1h)-one compounds | |
| EP0001098B1 (de) | Verfahren zur Herstellung von Morpholino-dithio-thiazolen | |
| JPS5965072A (ja) | インドリンまたはインドリン誘導体の製造方法 | |
| JPS604818B2 (ja) | 新規な２，６−ビス（アルキルアミノ）ピリジンまたはその塩およびそれらの製造法 | |
| US4013673A (en) | 2,3-dihydro-3-(2-pyridinyl)-4h-1-benzopyran-4-one n-oxides | |
| Fisher et al. | Some Anionic Cleavage Reactions of Alloxan | |
| JPS5750965A (en) | Preparation of n-methyl-4-benzazonine derivative | |
| JPS62292777A (ja) | 含フツ素クロマン類 | |
| JPS55130948A (en) | Asymmetric hydrogenation of alpha-aminoacrylic acid derivative | |
| JPS54112881A (en) | Preparation of 2-mercaptopyrimidine hydrochloride | |
| JPS5576863A (en) | Preparation of 2-chloronicotinic acid | |
| JPS5721387A (en) | Preparation of oxazolidinone derivative | |
| JPS63203631A (ja) | α−アリ−ルプロピオン酸の製造方法 |