HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1663329Generated: October 26, 2026
Water → 6-Chloro-1-(3,5-difluoro-benzyl)-1H-indole-3-carboxylic acid
https://huagongshe.com/reaction/1663329
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-[6-Chloro-1-(3,5-difluoro-benzyl)-1H-indol-3-yl]-2,2,2-trifluoro-ethanone | HCID 59756822 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 6-Chloro-1-(3,5-difluoro-benzyl)-1H-indole-3-carboxylic acid | HCID 59756704 | 95.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08034937B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-66dfe1b0c4964a5fae85338cf8e92a1d |
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| Source note | uspto-grants-2011_10 |
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