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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856816Generated: November 1, 2026

Sodium borohydride → 5-Amino-2-(3,3,3-trifluoropropyl)benzofuran

https://huagongshe.com/reaction/1856816

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22132946HCID 22132946—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-Amino-2-(3,3,3-trifluoropropyl)benzofuranHCID 22132957—

Reaction Steps

A mixture of 2.4 g (9.2 mmol) of 2-(3,3,3-trifluoropropyl)-5-nitrobenzofuran, 0.65 g (17 mmol) of sodium borohydride, 45 mg of Adogen® 464 (methyl trialkylammonium chloride) and 0.38 g of 5% palladium on carbon containing 50% of water in 95 ml of dichloromethane and 48 ml of water is stirred for 5 hours, then it is filtered on silica and the silica is rinsed with ethanol. The filtrate is then concentrated under reduced pressure and coevaporated with toluene. By chromatography of the residue on a silica column using a 0-30% mixture of ethyl acetate in cyclohexane, 2.0 g of product are obtained. Melting point: 74° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143772
Source datasetuspto-grants-2000_11
ORD IDord-1c3910b4c00042bc9275efe2f3d697e3
Source noteuspto-grants-2000_11