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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250821Generated: October 28, 2026

Trifluoroacetic acid → HCID 15550520, compound

https://huagongshe.com/reaction/1250821

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 15550519HCID 15550519—
SolventCarbon DisulfideHCID 6348—
ProductHCID 15550520HCID 1555052042%

Reaction Steps

Trifluoroacetic acid (30 mL) was added dropwise to a rt, stirred suspension of benzo[b]thiophen-2-yl-(2,3-dimethyl-furan-5-yl)-methanol (9.56 g, 40.0 mmol) and sodium borohydride (7.0 g, 200 mL) in carbon disulfide (100 mL) under a try N2 atmosphere over a period of 30 min. After an additional 3 hours, the reaction mixture was carefully quenched and further diluted with aqueous ammonium chloride (250 mL). Aqueous mixture was extracted with ethyl ether (500 mL). The ethyl ether extract was washed with water and brine. Silica gel (100 mL) was added. Solvents were removed and the silica adsorbate was flash chromatographed (eluent 99:1 petroleum ether:ethyl acetate) to provide the title compound as an oil (3.75 g, 42%): NMR (CDCl3); δ7.74 (d, J=8 Hz, 1H), 7.67 (d, J=8, Hz, 1H), 7.35-7.22 (m, 2H), 7.08 (d, J=1 Hz, 1H), 5.93 (s, 1H), 4.15 (s, 2H), 2.17 (s, 3H), 1.90 (s, 3H); MS (EI): [M+], 242.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340676B2
Source datasetuspto-grants-2002_01
ORD IDord-d6613821b4f04fed87fe2ce39821e191
Source noteuspto-grants-2002_01