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

HRID 546461
ノート
印刷プレビュー

反応式

HRID 546461 の反応式
[O:1]1[C@H:7]2[C@@H:2]1[CH2:3][C@H:4]([C:8]([O:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)=[O:9])[CH2:5][CH2:6]2.[Cl-].[NH4+].[N-:20]=[N+:21]=[N-:22].[Na+]>CN(C)C=O>[N:20]([C@H:7]1[CH2:6][CH2:5][C@@H:4]([C:8]([O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[O:9])[CH2:3][C@@H:2]1[OH:1])=[N+:21]=[N-:22]
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 57432601Benzyl (1R*,3S*,4R)-3,4-epoxycyclohexane-1-carboxylate

生成物 1

HCID 57462945Benzyl (1R*,3S*,4S*)-4-azido-3-hydroxycyclohexane-1-carboxylate収率 99.7%

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-dimethyl-formamide (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-49fa912d47a24a1da3b540867dce38a7
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07935824B2

反応ノート

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