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

Ammonium Chloride → Benzyl (1R*,3S*,4S*)-4-azido-3-hydroxycyclohexane-1-carboxylate

HRID 459517
ノート
印刷プレビュー

反応式

HRID 459517 の反応式
[O:1]1[CH:7]2[CH:2]1[CH2:3][CH:4]([C:8]([O-:10])=[O:9])[CH2:5][CH2:6]2.[Cl-].[NH4+].[N-:13]=[N+:14]=[N-:15].[Na+]>CN(C)C=O>[N:13]([C@H:7]1[CH2:6][CH2:5][C@@H:4]([C:8]([O:10][CH2:8][C:4]2[CH:5]=[CH:6][CH:7]=[CH:2][CH:3]=2)=[O:9])[CH2:3][C@@H:2]1[OH:1])=[N+:14]=[N-:15]
参加物反応条件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 25517Ammonium ChlorideHCID 33557Sodium AzideHCID 219323873,4-Epoxycyclohexane-1-carboxylate

生成物 1

HCID 57462945Benzyl (1R*,3S*,4S*)-4-azido-3-hydroxycyclohexane-1-carboxylate収率 121.2%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
70 °C

実験手順

Benzyl (1R*,3S*, 4R*)-3,4-epoxycyclohexane-1-carboxylate (52.3 g) was dissolved in N,N-dimethylformamide (1000 ml), ammonium chloride (21.9 g) and sodium azide (18.1 g) were added, and the mixture was heated to 70° C. and stirred for 24 hours. The solvent was distilled off under reduced pressure, and water was added to conduct extraction with ethyl acetate. The resultant organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure to obtain the title compound (61.8 g) as a colorless oil.

後処理

  1. distillationThe solvent was distilled off under reduced pressure, and water
  2. additionwas added
  3. extractionextraction with ethyl acetate
  4. washThe resultant organic layer was washed with saturated saline
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationThe solvent was distilled off under reduced pressure

出典と根拠

ORDレコード
ord-61f4cd57cd8141e4b1090ed046ea2a44
出典データセット
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07192968B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート