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Phosphorus tribromide → 4-(Bromomethyl)-3,5-dichloropyridine hydrobromide

HRID 577166
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HRID 577166 반응식
[Cl:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([Cl:10])[C:7]=1[CH2:8]O.[Br:11]P(Br)Br>ClCCl>[BrH:11].[Br:11][CH2:8][C:7]1[C:2]([Cl:1])=[CH:3][N:4]=[CH:5][C:6]=1[Cl:10]
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참가 물질

4

반응물 2

HCID 24614Phosphorus tribromideHCID 17855219(3,5-Dichloropyridin-4-yl)methanol

생성물 1

HCID 668153104-(Bromomethyl)-3,5-dichloropyridine hydrobromide수율 156.7%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of (3,5-dichloropyridin-4-yl)methanol (1.9 g, 10.7 mmol) in anhydrous dichloromethane (75 mL) was added tribromophosphane (1.1 mL, 11.5 mmol). The mixture was stirred at room temperature for 1.5 hours. Dichloromethane was evaporated, and the mixture was co-evaporated with toluene (2×20 mL). The residue was dried in vacuo, affording 4-(bromomethyl)-3,5-dichloropyridine hydrobromide (2.9 g, 98% yield), which was used without further purification.

후처리

  1. customDichloromethane was evaporated
  2. customThe residue was dried in vacuo

출처 및 근거

ORD 기록
ord-be2afbcb2c7a459583b1be10f1ac457a
출처 데이터셋
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09040538B2

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