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Triphenylphosphine → 3-Bromo-5-(bromomethyl)pyridine

HRID 712645
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HRID 712645 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH2:8]O)[CH:5]=[N:6][CH:7]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1C(=O)N([Br:36])C(=O)C1>C(Cl)Cl>[Br:1][C:2]1[CH:7]=[N:6][CH:5]=[C:4]([CH2:8][Br:36])[CH:3]=1
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참가 물질

5

반응물 3

HCID 11776TriphenylphosphineHCID 67184N-bromobutanimideHCID 2784733(5-Bromo-3-pyridinyl)methanol

생성물 1

HCID 149329483-Bromo-5-(bromomethyl)pyridine수율 67.2%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

(5-Bromo-pyridin-3-yl)-methanol (500 mg, 2.7 mmol) and triphenylphosphine (840 mg, 3.2 mmol) are dissolved in 12 mL of DCM and NBS (570 mg, 3.2 mmol) is added. The mixture is stirred for 4 hrs and then the reaction mixture is directly purified by flash column chromatography give 455 mg of 3-bromo-5-bromomethyl-pyridine.

후처리

  1. customthe reaction mixture is directly purified by flash column chromatography

출처 및 근거

ORD 기록
ord-f94edaf7e3f940ec97ec851b9df2b0a8
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09181272B2

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