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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034062Generated: October 30, 2026

Boron trifluoride etherate → Ethyl 4-[3-(3-nitrobenzyl)indol-1-yl]butyrate

https://huagongshe.com/reaction/1034062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantEthyl AcetateHCID 8857—
ReactantSodium borohydrideHCID 4311764—
ReactantEthyl 4-[3-(3-nitrobenzoyl)indol-1-yl]butyrateHCID 10547793—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-[3-(3-nitrobenzyl)indol-1-yl]butyrateHCID 1902473735.9%

Reaction Steps

To a solution of ethyl 4-[3-(3-nitrobenzoyl)indol-1-yl]butyrate (0.5 g) in tetrahydrofuran (10 ml) were added sodium borohydride (99.4 mg) and boron trifluoride etherate (0.485 ml) at -25° C., and the mixture was stirred at the same temperature for 2 hours. The mixture was poured into a mixture of ethyl acetate and ice water. The organic layer was separated, washed with water and brine, and dried over magnesium sulfate. After evaporation of the solvent, the residue was chromatographed on silica gel (25 g) eluting with a mixture of ethyl acetate and hexane (1:4) to give ethyl 4-[3-(3-nitrobenzyl)indol-1-yl]butyrate (173 mg) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05312829
Source datasetuspto-grants-1994_05
ORD IDord-823175a2c43048419750cd1056b5ade1
Source noteuspto-grants-1994_05