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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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Dichloromethane → HCID 12800846、化合物

HRID 1376845
ノート
印刷プレビュー

反応式

HRID 1376845 の反応式
C(Cl)Cl.S(C1C=CC(C)=CC=1)(O)(=O)=O.[NH2:15][CH2:16][C:17]([O:19][CH2:20][C:21]1[CH:26]=[CH:25][C:24]([N+:27]([O-:29])=[O:28])=[CH:23][CH:22]=1)=[O:18].[OH-].[Na+]>O>[NH2:15][CH2:16][C:17]([O:19][CH2:20][C:21]1[CH:26]=[CH:25][C:24]([N+:27]([O-:29])=[O:28])=[CH:23][CH:22]=1)=[O:18]
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 6344DichloromethaneHCID 14798Sodium HydroxideHCID 12800847p-Nitrobenzyl glycinate tosylate

生成物 1

HCID 12800846HCID 12800846、化合物収率 95.1%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A mixture of one liter of methylene chloride, 500 ml of water and 100 g of p-nitrobenzyl glycinate tosylate was strongly stirred while 26 ml of 10N sodium hydroxide were added dropwise and stirring was continued for 5 minutes after the addition. The decanted aqueous phase was extracted with methylene chloride and the combined organic phases were washed with water, dried and concentrated to dryness under reduced pressure at less than 40° C. to obtain 52.3 g of p-nitrobenzyl glycinate melting at 45°-50° C.

後処理

  1. additionwere added dropwise
  2. additionafter the addition
  3. extractionThe decanted aqueous phase was extracted with methylene chloride
  4. washthe combined organic phases were washed with water
  5. customdried
  6. concentrationconcentrated to dryness under reduced pressure at less than 40° C.

出典と根拠

ORDレコード
ord-b677f8981439420b8171b9c36c007c3c
出典データセット
uspto-grants-1997_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05663164

反応ノート

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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