HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889674Generated: October 31, 2026
Sodium borohydride → 3,5-Dichloro-N-(4-fluorobenzyl)-2-hydroxy-N-(4-(hydroxy(phenyl)methyl)benzyl)benzenesulfonamide
https://huagongshe.com/reaction/1889674
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-(4-Benzoylbenzyl)-3,5-dichloro-N-(4-fluorobenzyl)-2-hydroxybenzenesulfonamide | HCID 58531392 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,5-Dichloro-N-(4-fluorobenzyl)-2-hydroxy-N-(4-(hydroxy(phenyl)methyl)benzyl)benzenesulfonamide | HCID 58531599 | 91.5% |
Reaction Steps
To a solution of N-(4-benzoylbenzyl)-3,5-dichloro-N-(4-fluorobenzyl)-2-hydroxybenzenesulfonamide (15 mg, 0.028 mmol) in THF (0.15 mL) and ethanol (0.15 mL) at 0° C. was added sodium borohydride (4 mg, 0.11 mmol). The reaction mixture was stirred at 0° C. for 1 h. The solvents were removed in vacuo and resulting residue was purified by preparative HPLC to give the title compound (14 mg) as a white solid. MS (ESI): 527.9 (M−H2O)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501992B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-4107f305358d4527abd8143b6e28c44a |
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| Source note | uspto-grants-2013_08 |
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