racemic N-chloroacetylisovaline → Hydrochloric Acid

HRID 413352ノート

反応式

HRID 413352 の反応式
[Cl:1][CH2:2][C:3]([NH:5][C@:6]([C:10]([OH:12])=[O:11])([CH3:9])[CH2:7][CH3:8])=[O:4]>O>[Cl:1][CH2:2][C:3]([NH:5][C@:6]([C:10]([OH:12])=[O:11])([CH3:9])[CH2:7][CH3:8])=[O:4].[ClH:1]

参加物

4

反応物 1

HCID 12009800racemic N-chloroacetylisovaline

生成物 2

HCID 313Hydrochloric AcidHCID 12009800racemic N-chloroacetylisovaline

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

In a 2-liter round-bottomed flask equipped with a condenser and a magnetic stirrer were placed 70 g of the (R)-N-chloroacetylisovaline obtained from the enzymatic resolution of racemic N-chloroacetylisovaline, 696 ml of water, and 696 ml of concentrated hydrochloric acid. The resulting mixture was heated at reflux for 2.25 hours. The mixture was then cooled to room temperature and the solvent was removed using rotary evaporation yielding a solid residue. the residue was washed with dry acetone and then dried in a vacuum oven at 40° C. yielding a crude product. The crude product was esterified with methanol using the above-described procedure for preparation of (S)-isovaline methyl ester hydrochloride to give 47.52 g of the corresponding (R)-isovaline methyl ester hydrochloride.

後処理

  1. customIn a 2-liter round-bottomed flask equipped with a condenser and a magnetic stirrer

出典と根拠

ORDレコード
ord-75fa0f7a932b43b3a1e0cce363ed57ac
出典データセット
uspto-grants-2003_05
特許番号
US06566403B1

反応ノート

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