Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249154Generated: October 28, 2026

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

https://huagongshe.com/reaction/249154

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 numberUS05212320
Source datasetuspto-grants-1993_05
ORD IDord-d5b05f02ad3247ef84eb4ad05375a1f2
Source noteuspto-grants-1993_05