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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1594307Generated: November 4, 2026

Lithium borohydride → HCID 11328901, compound

https://huagongshe.com/reaction/1594307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 87452070HCID 87452070—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11328901HCID 1132890184.32%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of methyl N-[(4-bromo-5-chloro thien-2-yl)sulfonyl]-4,4,4,4′,4′,4′-hexafluorovalinate (1.45 g, 2.907 mmol) in THF (20 mL) was added lithium borohydride (LiBH4) (5.82 mL, 11.64 mmol) under N2 atmosphere at 0° C. The reaction was allowed to warm to 25° C. for 19 h. The reaction was cooled to 0° C., quenched with 2N HCl (slow addition), diluted in ether (40 mL) and the organic layer was washed sequentially with 1N aqueous HCl (10 mL), saturated aqueous NaHCO3 (10 mL) and brine (15 mL), then dried over MgSO4, filtered and concentrated to obtain a crude oil (1.3 g). The crude product was purified by the Biotage Flash™ 40 chromatography system, eluent: 1:6 EtOAc-hexanes, to afford 4-bromo-5-chloro-N-[3,3,3-trifluoro-1-(hydroxymethyl)-2-(trifluoromethyl)propyl]thiophene-2-sulfonamide as a white solid (1.13 g, 84.32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07300951B2
Source datasetuspto-grants-2007_11
ORD IDord-97261e1890054ec2a35905ccd8159dde
Source noteuspto-grants-2007_11