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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556355Generated: October 29, 2026

Water → 6-Hydroxy-benzo[d]isothiazole-3-carboxylic acid (4-fluoro-3-trifluoromethyl-phenyl)-amide

https://huagongshe.com/reaction/556355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantBoron tribromideHCID 25134—
Reactant6-Methoxy-benzo[d]isothiazole-3-carboxylic acid (4-fluoro-3-trifluoromethyl-phenyl)-amideHCID 66992942—
SolventDichloromethaneHCID 6344—
Product6-Hydroxy-benzo[d]isothiazole-3-carboxylic acid (4-fluoro-3-trifluoromethyl-phenyl)-amideHCID 136346628—

Reaction Conditions

Temperature45 °C

Reaction Steps

A suspension of 252 mg (0.68 mMol) 6-methoxy-benzo[d]isothiazole-3-carboxylic acid (4-fluoro-3-trifluoromethyl-phenyl)-amide in 15 ml CH2Cl2 is cooled in an ice-bath, then 20 ml of a 1 M solution of BBr3 in CH2Cl2 are added. The suspension is stirred for 3 days at 45° C., the resulting solution is cooled, poured into water and EtOAc, the aq. layer is separated off and extracted twice with EtOAc. The organic layers are washed twice with water and sat. NaHCO3, dried (Na2SO4) and concentrated. Chromatography (Combi Flash; acetone/hexane 1:95→2:3) gives the title compound: MS: [M−1]=355; TLC(hexane/acetone 2:1): Rf=0.46.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058276B2
Source datasetuspto-grants-2011_11
ORD IDord-dafc320054874d4db0ccd81830b58111
Source noteuspto-grants-2011_11