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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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L-(+)-Cysteine → HCID 57312911、化合物

HRID 1503175
ノート
印刷プレビュー

反応式

HRID 1503175 の反応式
[NH2:1][C@H:2]([C:5]([OH:7])=[O:6])[CH2:3][SH:4].[C:8]([O:12][CH2:13][CH3:14])(=[O:11])[CH:9]=O>O>[CH3:14][CH2:13][O:12][C:8]([CH:9]1[NH:1][CH:2]([C:5]([OH:7])=[O:6])[CH2:3][S:4]1)=[O:11]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 5862L-(+)-CysteineHCID 70211Ethyl oxoacetate

生成物 1

HCID 57312911HCID 57312911、化合物収率 29,313.199%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

L-Cysteine (60.4 g, 0.50 mmol) and ethyl glyoxylate (polymer, 47% toluene solution, 50.9 g, 0.234 mol) were added to water (150 ml), and the mixture was stirred at room temperature for 50 hours. The obtained solution was concentrated under reduced pressure, and the precipitated solid was collected by filtration. The obtained white solid (about 40 g) was suspended in water (100 ml), and the suspension was stirred for 16 hours at slurry state. The white crystals were collected by filtration, and dried under reduced pressure to give thiazolidine-2,4-dicarboxylic acid 2-ethyl ester as a white solid (30.08 g).

後処理

  1. concentrationThe obtained solution was concentrated under reduced pressure
  2. filtrationthe precipitated solid was collected by filtration
  3. stirringthe suspension was stirred for 16 hours at slurry state
  4. filtrationThe white crystals were collected by filtration
  5. customdried under reduced pressure

出典と根拠

ORDレコード
ord-12434506e2874cdbb5e2421ef6840927
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09212154B2

反応ノート

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