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L-Leucine → Benzoyl-L-leucine

HRID 1608116
ノート
印刷プレビュー

反応式

HRID 1608116 の反応式
[C:1](Cl)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[Na+].[NH2:12][C@H:13]([C:18]([OH:20])=[O:19])[CH2:14][CH:15]([CH3:17])[CH3:16]>O>[C:1]([NH:12][C@H:13]([C:18]([OH:20])=[O:19])[CH2:14][CH:15]([CH3:17])[CH3:16])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
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 6106L-LeucineHCID 7412Benzoyl chlorideHCID 14798Sodium Hydroxide

生成物 1

HCID 853887Benzoyl-L-leucine

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Benzoyl chloride (4.22 g, 0.030 mol) and 10% NaOH (12 ml, 0.030 mol) were added separately with vigorous stirring to a solution of L-leucine (3.94 g, 0.030 mol) in 150 ml of distilled water at ice bath temperature. The reaction was allowed to proceed at this temperature until the reaction mixture became clear (30 minutes); it was then extracted with ethyl acetate (2×100 ml). The aqueous layer was separated, acidified to pH 2 with 10% HCl, and extracted with ethyl acetate (3×50 ml). The ethyl acetate extract was dried over anhydrous sodium sulfate. After filtration, the filtrate was evaporated in vacuo to yield quantitative amount of N-benzoyl-L-leucine as a semi-solid which was used directly for the following step.

後処理

  1. custom(30 minutes)
  2. extractionit was then extracted with ethyl acetate (2×100 ml)
  3. customThe aqueous layer was separated
  4. extractionextracted with ethyl acetate (3×50 ml)
  5. extractionThe ethyl acetate extract
  6. dry with materialwas dried over anhydrous sodium sulfate
  7. filtrationAfter filtration
  8. customthe filtrate was evaporated in vacuo

出典と根拠

ORDレコード
ord-912f71e291cb4ac7808649629e534e6a
出典データセット
uspto-grants-1989_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04870056

反応ノート

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