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Water → 2,1-Benzisothiazole-4-methanol

HRID 1639849
Notes
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Reaction equation

HRID 1639849 reaction equation
[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
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

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%).

Workup

  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)

Sources & evidence

ORD record
ord-331d46093efd4e009b397c577a85067e
Source dataset
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08110585B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes