HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266892Generated: October 31, 2026
Borane;tetrahydrofuran → HCID 11348323, compound
https://huagongshe.com/reaction/2266892
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | HCID 68429208 | HCID 68429208 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11348323 | HCID 11348323 | 48% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07858658B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-77ee165e31034a61bdbb4433a3f199be |
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| Source note | uspto-grants-2010_12 |
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