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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231836Generated: October 25, 2026

Water → [2-(Trifluoromethyl)-1H-indol-3-yl]methanol

https://huagongshe.com/reaction/231836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantPotassium borohydrideHCID 4192641—
Reactant2-trifluoromethyl-3-formyl-(1H)-indoleHCID 20032128—
SolventDiethyl EtherHCID 3283—
Product[2-(Trifluoromethyl)-1H-indol-3-yl]methanolHCID 2003211364.6%

Reaction Steps

2 g of potassium borohydride were added in small fractions at +5° C. to a solution of 4.6 g of the product of Step A, 150 ml of tetrahydrofuran and 30 ml of water and the mixture was stirred for one hour. The mixture was allowed to return to ambient temperature and the tetrahydrofuran was eliminated under reduced pressure. The resulting mixture was diluted with ether, washed with water, dried and concentrated under reduced pressure. The residue was chromatographed over silica (eluent: hexaneethyl acetate 7-3) to obtain 3 g of 2-trifluoromethyl-(1H)-indol-3-yl methanol melting at 106° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04849443
Source datasetuspto-grants-1989_07
ORD IDord-ad967951fb5a48f7bfe9f3319054f3fa
Source noteuspto-grants-1989_07