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Phosphorus tribromide → 1-(Benzyloxy)-2-(bromomethyl)-4-chlorobenzene

HRID 2356600
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HRID 2356600 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[C:6]([CH2:8]O)[CH:7]=1.P(Br)(Br)[Br:19]>ClCCl>[C:12]1([CH2:11][O:10][C:5]2[CH:4]=[CH:3][C:2]([Cl:1])=[CH:7][C:6]=2[CH2:8][Br:19])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1
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참가 물질

4

반응물 2

HCID 24614Phosphorus tribromideHCID 19317759(2-Benzyloxy-5-chloro-phenyl)-methanol

생성물 1

HCID 221055531-(Benzyloxy)-2-(bromomethyl)-4-chlorobenzene

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

반응 조건

온도
-10 °C

실험 절차

{5-chloro-2-[(phenylmethyl)oxy]phenyl}methanol (8.2 g, 33 mmol) was dissolved in dry dichloromethane under nitrogen and cooled to −10° C. Phosphorus tribromide (3.12 ml, 33 mmol) in dry dichloromethane (15 ml) was added slowly. The mixture was left at −10° C. for 15 mins, then stirred at room temperature overnight. TLC showed no more starting material. The mixture was then quenched with a saturated sodium hydrogen carbonate solution added very slowly. The mixture was diluted with dichloromethane and brine was added to aid separation. The organic phase was washed with water (×2), then dried (MgSO4) and evaporated. The residue was purified (50 g SPE column). Product comes off using 5% ethyl acetate in isohexane. White-ish solid obtained (8.1 g).

후처리

  1. customThe mixture was then quenched with a saturated sodium hydrogen carbonate solution
  2. additionadded very slowly
  3. additionThe mixture was diluted with dichloromethane and brine
  4. additionwas added
  5. customseparation
  6. washThe organic phase was washed with water (×2)
  7. dry with materialdried (MgSO4)
  8. customevaporated
  9. customThe residue was purified (50 g SPE column)
  10. customWhite-ish solid obtained (8.1 g)

출처 및 근거

ORD 기록
ord-424a12a17d614faca7636c1244816676
출처 데이터셋
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07759369B2

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