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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760577Generated: October 31, 2026

Potassium Hydroxide → 7-(trifluoromethoxy)-1H-indole

https://huagongshe.com/reaction/1760577

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantCarbamic acid, N-[2-(trifluoromethoxy)-6-[2-(trimethylsilyl)ethynyl]phenyl]-, ethyl esterHCID 59133031—
Solventtert-ButanolHCID 6386—
Product7-(trifluoromethoxy)-1H-indoleHCID 22338244103.3%

Reaction Steps

Potassium hydroxide (17.9 g, 321 mmol) was boiled for 2 h in t-butanol (500 mL). (2-Trifluoromethoxy-6-trimethylsilanylethynyl-phenyl)-carbamic acid ethyl ester (52.8 g, 153 mmol) dissolved in t-butanol (500 mL) was added and boiling was continued for 2 h. The solvent was removed in vacuo and the residue was partitioned between diethyl ether and water. The organic phases were washed with brine, pooled and dried with MgSO4. Evaporation of the solvent yielded 31.8 g of brownish oil, which was purified by chromatography on silica gel with hexane/ethylacetate (9:1). This yielded the title compound, (30.2 g, 98%) as a yellow oil. (EI-MS: m/e=201.0 (M+)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06844345B2
Source datasetuspto-grants-2005_01
ORD IDord-1cdc17eadb534076a2bbd16f07bbc83d
Source noteuspto-grants-2005_01