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Water → 2,1-Benzisothiazole-4-methanol

HRID 1639849
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HRID 1639849 반응식
[N:1]1[S:2][CH:3]=[C:4]2[C:9]([C:10](OC)=[O:11])=[CH:8][CH:7]=[CH:6][C:5]=12.[H-].C([Al+]CC(C)C)C(C)C.O>O1CCCC1>[N:1]1[S:2][CH:3]=[C:4]2[C:9]([CH2:10][OH:11])=[CH:8][CH:7]=[CH:6][C:5]=12
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참가 물질

5

반응물 3

HCID 962WaterHCID 12255806Methyl benzo[c]isothiazole-4-carboxylateHCID 21225700Diisobutylaluminumhydride

생성물 1

HCID 593344662,1-Benzisothiazole-4-methanol수율 98.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of methyl 2,1-benzisothiazole-4-carboxylate (5.00 g, 25.9 mmol) in tetrahydrofuran (129 mL) was added diisobutylaluminum hydride (1 M hexane solution, 78.0 mL, 78.0 mmol) at −78° C., and the mixture was stirred at room temperature for 3 hr. The reaction solution was cooled to 0° C., and water was added. The mixture was extracted with ethyl acetate, washed with saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane=20/80) to give the title compound (4.2 g, yield 98%).

후처리

  1. temperatureThe reaction solution was cooled to 0° C.
  2. extractionThe mixture was extracted with ethyl acetate
  3. washwashed with saturated brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. customthe solvent was evaporated under reduced pressure
  6. customThe residue was purified by silica gel column chromatography (ethyl acetate/hexane=20/80)

출처 및 근거

ORD 기록
ord-331d46093efd4e009b397c577a85067e
출처 데이터셋
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08110585B2

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