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Boron tribromide → 4-Hydroxybenzothiazole

HRID 2220337
ノート
印刷プレビュー

反応式

HRID 2220337 の反応式
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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

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

生成物 1

HCID 819014-Hydroxybenzothiazole収率 156.3%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
40 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-a6f910b2831040b380d7ef2b23800210
出典データセット
uspto-grants-2008_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07417064B2

反応ノート

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