Sulfuric Acid → 3-Phenyllactic acid, (S)-

HRID 10912

反応式

HRID 10912 の反応式
N[C@H:2]([C:10]([OH:12])=[O:11])[CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.S(=O)(=O)(O)[OH:14].N([O-])=O.[Na+].COC(C)(C)C>O>[OH:14][C@@H:2]([CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1)[C:10]([OH:12])=[O:11]

参加物

6

反応条件

温度
20 °C

実験手順

L-Phenylalanine (10.00 g, 60.5 mmol) was added to a dilution of 8.88 g (90.5 mmol) of concentrated sulfuric acid in 110 g of water and then, at an inside temperature of 20° C., a mixture of 10.45 g (151.5 mmol) of sodium nitrite and 20 g of water was added over 5 hours. After addition, the mixture was stirred at 20° C. for 20 hours, 100 ml of t-butyl methyl ether was then added and, after 30 minutes of stirring at 20° C., the organic phase was separated (extract 1). Further, 50 ml of t-butyl methyl ether was added to the aqueous phase, the mixture was stirred at 20° C. for 30 minutes, and the organic phase was separated (extract 2). The extracts 1 and 2 were combined. The combined extract (116.5 g) contained 8.6 g of (2S)-2-hydroxy-3-phenylpropionic acid (yield 86%, optical purity 95.9% ee). The proton concentration (normality) in the reaction of this example was 1.7 mol/kg, the amount of the protonic acid was 3.0 equivalents (relative to L-phenylalanine), and the reaction temperature was 20° C.

後処理

  1. additionwas added over 5 hours
  2. additionAfter addition
  3. stirringof stirring at 20° C.
  4. customthe organic phase was separated
  5. extraction(extract 1)
  6. additionFurther, 50 ml of t-butyl methyl ether was added to the aqueous phase
  7. stirringthe mixture was stirred at 20° C. for 30 minutes
  8. customthe organic phase was separated
  9. extraction(extract 2)
  10. extractionThe combined extract (116.5 g)

出典と根拠

ORDレコード
ord-23c4a84d57fe4641be57dc04c183155c
出典データセット
uspto-grants-2006_08
特許番号
US07094926B2

関連ノート

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