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Benzyl chloroformate → HCID 117697513、化合物

HRID 1778510
ノート
印刷プレビュー

反応式

HRID 1778510 の反応式
Cl.[CH:2]12[NH:11][CH:6]([CH2:7][C:8](=[O:10])[CH2:9]1)[CH2:5][O:4][CH2:3]2.[C:12](Cl)([O:14][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[O:13]>ClCCl>[O:10]=[C:8]1[CH2:9][CH:2]2[N:11]([C:12]([O:14][CH2:15][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)=[O:13])[CH:6]([CH2:5][O:4][CH2:3]2)[CH2:7]1
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 10387Benzyl chloroformateHCID 716271383-Oxa-9-azabicyclo[3.3.1]nonan-7-one--hydrogen chloride (1/1)

生成物 1

HCID 117697513HCID 117697513、化合物収率 65.2%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

反応条件

温度
0 °C

実験手順

3-oxa-9-azabicyclo[3.3.1]nonan-7-one hydrochloride (CAS 1126795-00-3) (10 g) was dissolved in 200 ml of dichloromethane which was cooled to 0° C. Then, CbzCl (14.3 g, 84.7 mmol) was added to the mixture followed by the dropwise addition of a solution of TEA (14.6 ml, 112.8 mmol) in 20 ml of dichloromethane. The mixture was allowed to warm up to room temperature. After stirring 2 h, it was quenched with 20 ml of a saturated aqueous solution of NaHCO3. The two layers were separated and the aqueous layer was extracted with dichloromethane (3×150 ml). The combined organic layers were washed with water, dried over Na2SO4 and the solvent was evaporated under reduced pressure. The crude product was purified by chromatography on silica gel, yielding 10.1 g of benzyl 7-oxo-3-oxa-9-azabicyclo[3.3.1]nonane-9-carboxylate 100b (64%).

後処理

  1. temperatureto warm up to room temperature
  2. customit was quenched with 20 ml of a saturated aqueous solution of NaHCO3
  3. customThe two layers were separated
  4. extractionthe aqueous layer was extracted with dichloromethane (3×150 ml)
  5. washThe combined organic layers were washed with water
  6. dry with materialdried over Na2SO4
  7. customthe solvent was evaporated under reduced pressure
  8. customThe crude product was purified by chromatography on silica gel

出典と根拠

ORDレコード
ord-21761757798f44a291b1aaf2187accea
出典データセット
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09266904B2

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