Benzyl chloroformate → Benzyl 3-(hydroxymethyl)azepane-1-carboxylate

HRID 1246920ノート

反応式

HRID 1246920 の反応式
C(=O)([O-])[O-].[K+].[K+].[NH:7]1[CH2:13][CH2:12][CH2:11][CH2:10][CH:9]([CH2:14][OH:15])[CH2:8]1.[CH2:16]([O:23][C:24](Cl)=[O:25])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>C1COCC1.O>[CH2:16]([O:23][C:24]([N:7]1[CH2:13][CH2:12][CH2:11][CH2:10][CH:9]([CH2:14][OH:15])[CH2:8]1)=[O:25])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1

参加物

5

反応物 3

HCID 10387Benzyl chloroformateHCID 11430Potassium CarbonateHCID 21901984(Azepan-3-yl)methanol

生成物 1

HCID 20598086Benzyl 3-(hydroxymethyl)azepane-1-carboxylate収率 94%

試薬・触媒・溶媒 1

HCID 21881883Oxolane--water (1/1)溶媒

反応条件

温度
0 °C

実験手順

Potassium carbonate was added to a mixture of azepan-3-yl-methanol (145) (0.032 g, 0.2485 mmol) in THF/H2O (2:1, 0.31 mL). The suspension was cooled to 0° C., and (benzyloxy)carbonyl chloride (0.071 mL, 0.497 mmol) was added dropwise. The reaction was allowed to warm to room temperature overnight, and was then concentrated in vacuo. CH2Cl2 and H2O were added. The organics were extracted, washed with brine, dried over sodium sulfate, filtered and concentrated in vacuo. The crude material was purified by automated silica gel chromatography with 75:25 Hexanes:EtOAc to obtain 3-Hydroxymethyl-azepan-1-carboxylic acid benzyl ester (146) in approximately 94% yield.

後処理

  1. temperatureto warm to room temperature overnight
  2. concentrationwas then concentrated in vacuo
  3. additionCH2Cl2 and H2O were added
  4. extractionThe organics were extracted
  5. washwashed with brine
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customThe crude material was purified by automated silica gel chromatography with 75:25 Hexanes

出典と根拠

ORDレコード
ord-71500117350e40bf885c8952e0a52074
出典データセット
uspto-grants-2006_10
特許番号
US07129228B2

反応ノート

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