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Phosphorus tribromide → HCID 19861650, 화합물

HRID 1165415
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HRID 1165415 반응식
P(Br)(Br)[Br:2].[Br:5][C:6]1[C:7]([CH2:16]O)=[CH:8][C:9]2[C:14]([CH:15]=1)=[CH:13][CH:12]=[CH:11][CH:10]=2>C(OCC)C>[Br:5][C:6]1[C:7]([CH2:16][Br:2])=[CH:8][C:9]2[C:14]([CH:15]=1)=[CH:13][CH:12]=[CH:11][CH:10]=2
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참가 물질

4

반응물 2

HCID 24614Phosphorus tribromideHCID 264948(3-bromonaphthalen-2-yl)methanol

생성물 1

HCID 19861650HCID 19861650, 화합물

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

PBr3 (3.7 mL, 0.039 mol) was added dropwise to a suspension of 3-bromo-2-naphthalenyl methanol (8.55 g, 0.036 mol) and diethyl ether (80 mL) at 0° C. After 1 hour, the reaction was concentrated and partitioned between CH2Cl2 and H2O. The organic layer was separated and dried over MgSO4. Concentration in vacuo afforded 3-bromo-2-bromomethylnaphthalene as a crude product (10.6 g). The crude product was flash chromatographed on silica gel to afford the pure product as an off-white powder (6.0 g, m.p. 110°-111° C., yield 56%).

후처리

  1. concentrationthe reaction was concentrated
  2. custompartitioned between CH2Cl2 and H2O
  3. customThe organic layer was separated
  4. dry with materialdried over MgSO4
  5. concentrationConcentration in vacuo

출처 및 근거

ORD 기록
ord-95b623ee845b4e4bb3f70767464c035d
출처 데이터셋
uspto-grants-1990_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04910019

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