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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402684Generated: November 1, 2026

Hydrochloric Acid → 7-(Trifluoromethyl)-1H-indole

https://huagongshe.com/reaction/2402684

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBoron trifluoride etherateHCID 8000—
Reactant7-TrifluoromethylisatinHCID 604575—
ReactantSodium borohydrideHCID 4311764—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product7-(Trifluoromethyl)-1H-indoleHCID 10419882—

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a stirred mixture of 7-trifluoromethyl-1H-indole-2,3-dione (116 mg) in THF (5.00 mL) was added boron trifluoride etherate (0.205 mL, 1.62 mmol) followed by sodium borohydride (71.4 mg, 1.88 mmol). The resulting mixture was stirred at −20° C. for 2 hrs, then water (1 mL) was added and the mixture was stirred at 0° C. for 10 min. The solution was acidified to pH=1 with 2N HCl, warmed to r.t. and stirred at r.t. for 20 min prior to extraction with EtOAc. The extracts were dried over magnesium sulphate, concentrated in vacuo and the residue purified by chromatography over silica gel eluting with hexane to give 7-trifluoromethyl-1H-indole. 1H NMR (400 MHz, CDCl3) δ ppm 6.63-6.68 (1H, m), 7.20 (1H, t, J=7.71 Hz), 7.30-7.35 (1H, m), 7.47 (1H, d, J=7.33 Hz), 7.83 (1H, d, J=8.08 Hz), and 8.56 (1H, br. s.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796455B2
Source datasetuspto-grants-2014_08
ORD IDord-7ba51afc543b45b5af0795af3c74c072
Source noteuspto-grants-2014_08