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Boron tribromide → 4-Hydroxybenzothiazole

HRID 2220337
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HRID 2220337 반응식
B(Br)(Br)Br.C[O:6][C:7]1[C:12]2[N:13]=[CH:14][S:15][C:11]=2[CH:10]=[CH:9][CH:8]=1>C(Cl)Cl>[OH:6][C:7]1[C:12]2[N:13]=[CH:14][S:15][C:11]=2[CH:10]=[CH:9][CH:8]=1
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참가 물질

4

반응물 2

HCID 25134Boron tribromideHCID 126318584-Methoxy-1,3-benzothiazole

생성물 1

HCID 819014-Hydroxybenzothiazole수율 156.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
40 °C

실험 절차

Boron tribromide (3.09 ml, 1M solution in DCM, 3.09 mmol) was added dropwise at 0° C. to a stirred solution of 4-methoxy-benzothiazole (510 mg, 3.09 mmol) in dry DCM (30ml). The resulting solution was warmed to 40° C. and allowed to stir overnight. The resulting solution was concentrated in vacuo and diluted with water and HCl (2N). The aqueous phase was neutralised to pH˜7 with NaHCO3 and the solution extracted with EtOAc (3×100 ml) and the combined organic extracts dried (MgSO4) and the solvent removed in vacuo. The resulting oil was purified by flash chromatography eluting silica gel with hexane:EtOAc [4:1] to hexane:EtOAc [7:3] to give the title compound as a tan solid (730 mg, 80%); δH (300 MHz, CDCl3) 7.59 (1H, s, CH), 7.46 (1H, dd, Ar), 7.36 (1H, t, Ar), 7.02 (1H, dd, Ar).

후처리

  1. concentrationThe resulting solution was concentrated in vacuo
  2. additiondiluted with water and HCl (2N)
  3. extractionthe solution extracted with EtOAc (3×100 ml)
  4. dry with materialthe combined organic extracts dried (MgSO4)
  5. customthe solvent removed in vacuo
  6. customThe resulting oil was purified by flash chromatography
  7. washeluting silica gel with hexane

출처 및 근거

ORD 기록
ord-a6f910b2831040b380d7ef2b23800210
출처 데이터셋
uspto-grants-2008_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07417064B2

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