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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266892Generated: October 31, 2026

Borane;tetrahydrofuran → HCID 11348323, compound

https://huagongshe.com/reaction/2266892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorane;tetrahydrofuranHCID 2723981—
ReactantHCID 68429208HCID 68429208—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11348323HCID 1134832348%

Reaction Conditions

Temperature25 °C

Reaction Steps

Borane-THF (1 M, 15 mL, 14.21 mmol) was added dropwise over 30 min at 0° C. to a solution of N-[(5-chlorothien-2-yl)sulfonyl]-5,5,5-trifluoronorvaline (1.0 g, 2.84 mmol) in THF (10 mL). The reaction was allowed to warm to 25° C. for 18 h and then was quenched by addition of 50 mL of 10% acetic acid in methanol. After solvent evaporation, the crude product was dissolved in EtOAc and washed with 1N HCl, H2O and saturated NaHCO3. The organic layer was dried over MgSO4, filtered and concentrated to produce a crude oil (0.83 g) that was purified via flash chromatography, eluent: 1:6 ethyl acetate-hexane. This produced the title compound 5-chloro-N-[4,4,4-trifluoro-1-(hydroxymethyl)butyl]thiophene-2-sulfonamide as a colorless oil (0.46 g, 48%). Mass Spectrum (−ESI): 337 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858658B2
Source datasetuspto-grants-2010_12
ORD IDord-77ee165e31034a61bdbb4433a3f199be
Source noteuspto-grants-2010_12