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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666951Generated: October 26, 2026

Water → 6-Chloro-1-(3,5-difluoro-benzyl)-1H-indole-3-carboxylic acid

https://huagongshe.com/reaction/1666951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant1-[6-Chloro-1-(3,5-difluoro-benzyl)-1H-indol-3-yl]-2,2,2-trifluoro-ethanoneHCID 59756822—
SolventDimethylformamideHCID 6228—
Solventtert-Butyl methyl etherHCID 15413—
Product6-Chloro-1-(3,5-difluoro-benzyl)-1H-indole-3-carboxylic acidHCID 5975670495.6%

Reaction Steps

To a solution of 2.2 g (6.5 mmol) 1-[6-chloro-1-(3,5-difluoro-benzyl)-1H-indol-3-yl]-2,2,2-trifluoro-ethanone in 65 ml DMF were added 1.7 g (36 mmol) sodium hydride (50% in oil) at room temperature. After stirring for 5 min. 0.59 ml (33 mmol) water were added dropwise. Stirring was continued at room temperature for 45 min. The reaction mixture was diluted with 150 ml of tert-butyl methyl ether and extracted with two 150-ml portions of a 1 M aqueous solution of sodium hydroxide. The combined aqueous layers were acidified to pH 1 with concentrated hydrochloric acid solution and extracted with three 150-ml portions of ethyl acetate. The combined organic extracts were dried over sodium sulfate, filtered and concentrated in vacuo. The residue was dried in high vacuo at 80° C. to give 2.0 g (95%) of the crude title compound as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044202B2
Source datasetuspto-grants-2011_10
ORD IDord-9f16f34957944c938df6553a8cb4d257
Source noteuspto-grants-2011_10