ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
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
  1. ホーム
  2. /反応

Water → N-(Bromoacetyl)glycine, ethyl ester

HRID 240321
ノート
印刷プレビュー

反応式

HRID 240321 の反応式
Cl.[CH2:2]([O:4][C:5](=[O:8])[CH2:6][NH2:7])[CH3:3].C([O-])([O-])=O.[K+].[K+].[Br:15][CH2:16][C:17](Br)=[O:18].O>C(Cl)Cl>[CH2:2]([O:4][C:5](=[O:8])[CH2:6][NH:7][C:17](=[O:18])[CH2:16][Br:15])[CH3:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 61147Bromoacetyl bromideHCID 2723640Glycine ethyl ester, hydrochloride

生成物 1

HCID 96555N-(Bromoacetyl)glycine, ethyl ester収率 40%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To a mixture of glycine ethyl ester hydrochloride (2.0 g, 14.3 mmol) and K2CO3 (2.1 g, 15.2 mmol) in CH2Cl2 (35 ml) cooled at 0-5° C. bromoacetyl bromide (1.36 ml, 15.6 mmol) was added dropwise. The suspension was stirred at room temperature and after 3 h H2O (20 ml) was added. The phases were separated and the organic one was washed with a saturated solution of NaHCO3 (20 ml) and H2O (20 ml) and dried over Na2SO4. The solvent was evaporated obtaining 39 as white solid (1.2 g, 40%). ESI+MS: calcd for C6H10BrNO3: 224.06; found: 224.0 and 226.0 (MH+).

後処理

  1. additionwas added dropwise
  2. additionwas added
  3. customThe phases were separated
  4. washthe organic one was washed with a saturated solution of NaHCO3 (20 ml) and H2O (20 ml)
  5. dry with materialdried over Na2SO4
  6. customThe solvent was evaporated

出典と根拠

ORDレコード
ord-85f3c0cf834d41b9a0e7d9c94b7c9c19
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08648076B2

反応ノート

読み込み中…

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