Toluene → N-[(S)-alpha-methylbenzyl]-(RS)-proline methyl ester

HRID 565721ノート

反応式

HRID 565721 の反応式
Br[CH:2]([CH2:7][CH2:8][CH2:9]Br)[C:3]([O:5][CH3:6])=[O:4].C1(C)C=CC=CC=1.C(=O)([O-])[O-].[K+].[K+].[CH3:24][C@H:25]([NH2:32])[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>O>[CH3:6][O:5][C:3](=[O:4])[CH:2]1[CH2:7][CH2:8][CH2:9][N:32]1[C@@H:25]([CH3:24])[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1

参加物

6

反応物 4

HCID 1140TolueneHCID 11430Potassium CarbonateHCID 758181-Phenethylamine, (-)-HCID 10912698Methyl 2,5-dibromopentanoate

生成物 1

HCID 11160639N-[(S)-alpha-methylbenzyl]-(RS)-proline methyl ester収率 78.1%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Methyl (RS)-2,5-dibromovalerate (24.5 g) and toluene (19.8 g) were added to a 49% aqueous potassium carbonate solution (53.3 g), and heated to 80° C. (S)-α-methylbenzylamine (12.0 g) was added dropwise to the mixture obtained above at that temperature, and was stirred at that temperature for 9.5 hours. Water (33.9 g) was added to the reaction mixture, and then the organic layer was separated from the resulting mixture. Separated organic layer was washed with water, a 1% aqueous hydrochloric acid solution and water in this order, and concentrated under reduced pressure. Thus, N-[(S)-α-methylbenzyl]-(RS)-proline methyl ester (16.3 g) was obtained in a yield of 77.8%.

後処理

  1. additionwas added dropwise to the mixture
  2. customobtained above at that temperature
  3. customthe organic layer was separated from the resulting mixture
  4. washSeparated organic layer was washed with water
  5. concentrationa 1% aqueous hydrochloric acid solution and water in this order, and concentrated under reduced pressure

出典と根拠

ORDレコード
ord-7af25a2137c0452f8a652c5f117e123a
出典データセット
uspto-grants-2001_01
特許番号
US06172234B2

反応ノート

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