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Benzene → isopropyl (2RS,3S)-3-amino-2-hydroxy-5-methylhexanoate hydrochloride

HRID 542372
ノート
印刷プレビュー

反応式

HRID 542372 の反応式
[ClH:1].[NH2:2][C@@H:3]([CH2:9][CH:10]([CH3:12])[CH3:11])[CH:4]([OH:8])[C:5]([OH:7])=[O:6].[CH:13]1[CH:18]=CC=C[CH:14]=1>C(O)(C)C>[ClH:1].[NH2:2][C@@H:3]([CH2:9][CH:10]([CH3:12])[CH3:11])[CH:4]([OH:8])[C:5]([O:7][CH:13]([CH3:18])[CH3:14])=[O:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 241BenzeneHCID 313Hydrochloric AcidHCID 12879199(2RS,3S)-3-amino-2-hydroxy-5-methylhexanoic acid

生成物 1

HCID 13913909isopropyl (2RS,3S)-3-amino-2-hydroxy-5-methylhexanoate hydrochloride

試薬・触媒・溶媒 1

HCID 3776Isopropanol溶媒

実験手順

Hydrogen chloride was passed into a solution of 4.0 g of (2RS, 3S)-3-amino-2-hydroxy-5-methylhexanoic acid in 50 ml of isopropyl alcohol with stirring under ice-cooling, and then 100 ml of dry benzene was added to the reaction mixture, and the mixture was heated under reflux for 10 minutes while removing water formed during the reaction using a molecular sieve. The reaction mixture was evaporated to dryness under reduced pressure to obtain 5.7 g of isopropyl (2RS, 3S)-3-amino-2-hydroxy-5-methylhexanoate hydrochloride as a white powder.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperaturecooling
  2. temperaturethe mixture was heated
  3. temperatureunder reflux for 10 minutes
  4. customwhile removing water
  5. customformed during the reaction
  6. customThe reaction mixture was evaporated to dryness under reduced pressure

出典と根拠

ORDレコード
ord-fbb099bf2a3f488d9c01b1ec0839721b
出典データセット
uspto-grants-1987_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04656269

反応ノート

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