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Phosphorus tribromide → 1-(Bromomethyl)-2-chloro-4-[(phenylmethyl)oxy]benzene

HRID 1946369
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HRID 1946369 반응식
[Cl:1][C:2]1[CH:7]=[C:6]([O:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:5]=[CH:4][C:3]=1[CH2:16]O.P(Br)(Br)[Br:19].C(=O)([O-])O.[Na+]>C(Cl)Cl>[Br:19][CH2:16][C:3]1[CH:4]=[CH:5][C:6]([O:8][CH2:9][C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)=[CH:7][C:2]=1[Cl:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 24614Phosphorus tribromideHCID 516892Sodium BicarbonateHCID 18443682HCID 18443682, 화합물

생성물 1

HCID 667704731-(Bromomethyl)-2-chloro-4-[(phenylmethyl)oxy]benzene수율 95.2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매3회

실험 절차

To a solution of {2-chloro-4-[(phenylmethyl)oxy]phenyl}methanol (2.08 g, 8.36 mmol) in DCM (20 ml) under nitrogen in an ice-water bath was added a solution of phosphorus tribromide (0.83 ml, 8.80 mmol, Aldrich) in DCM (10 ml). The solution was allowed to warm to ambient temperature and stirred for 1.5 h. The reaction mixture was poured onto ice-water (70 ml) and saturated aqueous sodium hydrogen carbonate (30 ml). The mixture was diluted with DCM (50 ml), and the phases separated. The aqueous extract was washed with dichloromethane (20 ml). The combined organic extracts were washed with water (50 ml), dried (MgSO4), filtered and the solvent removed in vacuo to give 1-(bromomethyl)-2-chloro-4-[(phenylmethyl)oxy]benzene as white solid (2.48 g).

후처리

  1. customthe phases separated
  2. extractionThe aqueous extract
  3. washwas washed with dichloromethane (20 ml)
  4. washThe combined organic extracts were washed with water (50 ml)
  5. dry with materialdried (MgSO4)
  6. filtrationfiltered
  7. customthe solvent removed in vacuo

출처 및 근거

ORD 기록
ord-1cffec4b81194c34ac8ec5ba08885e9c
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08399436B2

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