HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990600Generated: October 31, 2026
Hydrochloric Acid → 2-Fluoro-5-oxiranyl-benzenesulfonamide
https://huagongshe.com/reaction/990600
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-(2-Bromoacetyl)-2-fluorobenzenesulphonamide | HCID 11808590 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-Fluoro-5-oxiranyl-benzenesulfonamide | HCID 10987712 | 48.7% |
Reaction Steps
A solution of 0.5 g (1.7 mmol) of 5-bromoacetyl-2-fluoro-benzenesulfonamide V in 20 mL MeOH was cooled to 0° C. NaBH4 26 mg (0.67 mmol) was added and the reaction was stirred at 0° C. for 15 min. 4 mL of 1N NaOH was added and the reaction was stirred at 0° C. for 4 hrs. The reaction was adjusted to pH 6 by addition of dilute HCl. The volatiles were evaporated and the residue dissolved in EtOAc, washed with H2O, dried over Na2SO4 and evaporated. The product was purified by column chromatography on silica gel eluting with CH2Cl2/MeOH::9/1 to give 180 mg of VI (48%); mp 100-103° C.TLC:CH2Cl2/MeOH::9/1 single-spot material Rƒ 0.65.1H-NMR (300 MHz DMSO-D6) δ: (2.82, m, 1H), (3.14, m, 1H), (4.06, m, 1H), (7.40, t, 1H), (7.56, m, 1H), (7.66, m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06461822B2 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-7d630e878c6b4ee3b761c84695749569 |
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| Source note | uspto-grants-2002_10 |
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