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Water → 2-(2,4-Dichlorophenoxy)benzyl bromide

HRID 397837
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HRID 397837 반응식
P(Br)(Br)[Br:2].[Cl:5][C:6]1[CH:20]=[C:19]([Cl:21])[CH:18]=[CH:17][C:7]=1[O:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[CH2:15]O.O>O1CCOCC1.C(OCC)(=O)C>[Cl:5][C:6]1[CH:20]=[C:19]([Cl:21])[CH:18]=[CH:17][C:7]=1[O:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[CH2:15][Br:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 962WaterHCID 24614Phosphorus tribromide2회HCID 2763668[2-(2,4-Dichlorophenoxy)phenyl]methanol

생성물 1

HCID 230012632-(2,4-Dichlorophenoxy)benzyl bromide수율 57.3%

시약·촉매·용매 2

HCID 8857Ethyl Acetate용매HCID 312751,4-Dioxane
용매

실험 절차

Phosphorus(III) tribromide (0.41 ml, 4.37 mmol) was added to a solution of 1-[2-(2,4-dichlorophenoxy)phenyl]methanol (420 mg, 1.56 mmol) in dioxane (10 ml). The reaction mixture was stirred for 1 hour at room temperature. Another portion of phosphorus(III) tribromide (0.41 ml, 4.37 mmol) was added. The reaction mixture was stirred for 16 hours at room temperature. It was cooled to 0° C. Water (5 ml) was added dropwise. The reaction mixture was warmed to room temperature and diluted with ethyl acetate (400 ml). It was washed with a 10% aqueous solution of sodium hydrogensulphate. The aqueous phase was extracted with ethyl acetate (50 ml). The combined organic layers were washed with a saturated aqueous solution of sodium hydrogencarbonate (200 ml) and dried over magnesium sulphate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (100 g), using ethyl acetate/heptane 1:3 as eluent, to give 297 mg of 2-(2,4-dichlorophenoxy)benzyl bromide.

후처리

  1. stirringThe reaction mixture was stirred for 16 hours at room temperature
  2. temperatureIt was cooled to 0° C
  3. temperatureThe reaction mixture was warmed to room temperature
  4. washIt was washed with a 10% aqueous solution of sodium hydrogensulphate
  5. extractionThe aqueous phase was extracted with ethyl acetate (50 ml)
  6. washThe combined organic layers were washed with a saturated aqueous solution of sodium hydrogencarbonate (200 ml)
  7. dry with materialdried over magnesium sulphate
  8. customThe solvent was removed in vacuo
  9. customThe crude product was purified by flash chromatography on silica (100 g)

출처 및 근거

ORD 기록
ord-6908f7e111b5421792b182b6f382cb88
출처 데이터셋
uspto-grants-2003_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06610721B2

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