HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837002Generated: November 1, 2026
Sodium borohydride → HCID 22137849, compound
https://huagongshe.com/reaction/1837002
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Tetrahydrofuran ethanol | HCID 21873804 | — |
| Reactant | HCID 69592521 | HCID 69592521 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22137849 | HCID 22137849 | 54.3% |
Reaction Steps
To a THF/ethanol(10:1) solution of 3-(2-Phenylsulfanyl-acetylamino)-5-trifluoromethyl-benzoic acid methyl ester (252 mg, 0.68 mmol) was added sodium borohydride (46 mg, 1.4 mmol), and the mixture was stirred at 65° C. for 2 hours. The reaction mixture was left overnight. The mixture was diluted with ethyl acetate, washed with 1 N HCl (2×) and brine. The organic layer was dried over MgSO4, filtered and stripped. The crude product was purified by flash chromatography on silica gel eluted with hexane/ethyl acetate (4:1) to give 126 mg of N-(3-Hydroxymethyl-5-trifluoromethyl-phenyl)-2-phenylsulfanyl-acetamide in 54% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06780858B2 |
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| Source dataset | uspto-grants-2004_08 |
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| ORD ID | ord-00dececac68340a89498483acfb5ea10 |
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| Source note | uspto-grants-2004_08 |
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