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Sodium Azide → HCID 86607259、化合物

HRID 1437379
ノート
印刷プレビュー

反応式

HRID 1437379 の反応式
[CH3:1][O:2][C:3]([C@@H:5]1[CH2:10][CH2:9][C@H:8](Br)[C@H:7]([OH:12])[CH2:6]1)=[O:4].[N-:13]=[N+:14]=[N-:15].[Na+]>CN(C=O)C>[CH3:1][O:2][C:3]([C@@H:5]1[CH2:10][CH2:9][C@@H:8]([N:13]=[N+:14]=[N-:15])[C@H:7]([OH:12])[CH2:6]1)=[O:4]
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

4

反応物 2

HCID 33557Sodium AzideHCID 15640156HCID 15640156、化合物

生成物 1

HCID 86607259HCID 86607259、化合物収率 42%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
60 °C

実験手順

A solution of bromide (a) (52.4 g, 221 mmol) in DMF (1.2 liters) was treated with sodium azide (21.5 g, 331 mmol) and heated at 60° C. for 8 hours. The mixture was stirred at room temperature overnight and then evaporated. The residue was extracted with warm iso-propanol (2×300 ml). Evaporation afforded an oil which was chromatographed on silica eluting with a gradient of ethyl acetate in petroleum ether affording an oil (31 g) which was a 2:1 mixture of desired (1R,3R,4R)-4-azido-3-hydroxy-cyclohexanecarboxylic acid methyl ester to (R)-3-oxo-cyclohexanecarboxylic acid methyl ester. Further chromatography on silica eluting with a methanol/dichloromethane gradient afforded the desired intermediate as an oil (18.4 g, 42%)

後処理

  1. customevaporated
  2. extractionThe residue was extracted with warm iso-propanol (2×300 ml)
  3. customEvaporation
  4. customafforded an oil which
  5. customwas chromatographed on silica eluting with a gradient of ethyl acetate in petroleum ether affording an oil (31 g) which
  6. additiona 2:1 mixture of desired (1R,3R,4R)-4-azido-3-hydroxy-cyclohexanecarboxylic acid methyl ester to (R)-3-oxo-cyclohexanecarboxylic acid methyl ester

出典と根拠

ORDレコード
ord-e62e2f416a004abb9819ab97cbc31bbb
出典データセット
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07622481B2

反応ノート

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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