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Sodium Azide → 2-Azido-1,1-diphenylpropanol

HRID 974202
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HRID 974202 반응식
[C:1]1([C:7]2([C:11]3[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=3)[CH:9]([CH3:10])[O:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[N-:17]=[N+:18]=[N-:19].[Na+]>CN(C)C=O.O>[N:17]([CH:9]([CH3:10])[C:7]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)[OH:8])=[N+:18]=[N-:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 33557Sodium AzideHCID 110958912,2-Diphenyl-3-methyloxirane

생성물 1

HCID 150100222-Azido-1,1-diphenylpropanol수율 70%

시약·촉매·용매 1

HCID 21962138N,N-Dimethylformamide--water (1/1)용매

실험 절차

A solution of 9.35 g (44.5 mmol) 2,2-diphenyl-3-methyloxirane and 9.00 g (138 mmol) NaN3 in 100 ml of 2:1 N,N-dimethylformamide-water was heated at reflux for 72 hours. The solution was concentrated and the residue was partitioned between ether and water. The ether layer was washed with NaHCO3, then water, dried over Na2SO4 and concentrated. HPLC (5% EtOAc-hexane) afforded 7.86 g (70%) of 2-azido-1,1-diphenylpropanol as a clean oil.

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후처리

  1. temperatureat reflux for 72 hours
  2. concentrationThe solution was concentrated
  3. customthe residue was partitioned between ether and water
  4. washThe ether layer was washed with NaHCO3
  5. dry with materialwater, dried over Na2SO4
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-ec5743d28da24c2d97d957c9eb0db650
출처 데이터셋
uspto-grants-1991_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05068248

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