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6-Bromo-2-naphthalenol → 6-Bromo-1-fluoronaphthalen-2-OL

HRID 1925244
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HRID 1925244 반응식
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[CH:8]=[C:7]([OH:12])[CH:6]=[CH:5]2.C1C=CC(S(N(S(C2C=CC=CC=2)(=O)=O)[F:23])(=O)=O)=CC=1>CN(C=O)C>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8]([F:23])=[C:7]([OH:12])[CH:6]=[CH:5]2
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참가 물질

4

반응물 2

HCID 271446-Bromo-2-naphthalenolHCID 588007N-Fluorobenzenesulfonimide

생성물 1

HCID 112419406-Bromo-1-fluoronaphthalen-2-OL

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of 6-bromo-naphthalen-2-ol (5 g, 22.4 mmol, Aldrich) in dry DMF (50 mL, Aldrich) was added N-fluorobenzene sulfonimide (21.9 g, 67.2 mmol, Aldrich). The reaction was stirred at RT for 48 h. The volatile portion was removed in vacuo and the residue was purified by silica gel chromatography (CHCl3) to give title compound as a yellow solid. MS (ESI, neg. ion) m/z: 240.0 (M−1). Mass Calc'd for C10H6BrFO: 239.96.

후처리

  1. customThe volatile portion was removed in vacuo
  2. customthe residue was purified by silica gel chromatography (CHCl3)

출처 및 근거

ORD 기록
ord-daa60531c2344fb39691cc2cd7b9cc5f
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08178557B2

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