HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83905Generated: October 30, 2026
Sodium Sulfite → 2-Chloro-6-fluoro-4-sulfamoylbenzyl acetate
https://huagongshe.com/reaction/83905
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 4-Amino-2-chloro-6-fluorobenzyl acetate | HCID 66740368 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Chloro-6-fluoro-4-sulfamoylbenzyl acetate | HCID 66740199 | 15.1% |
Reaction Steps
To a solution of 4-amino-2-chloro-6-fluorobenzyl acetate (5.2 g, 0.024 mol) in DMF (10 mL) at 0° C. was added slowly 3M HCl (100 mL) followed by NaNO2 (2 g, 0.029 mol). After stirring at the same temperature for 20 min, the mixture was added dropwise to a solution of Na2SO3 (12 g, 0.096 mol) and CuSO45H2O in 3N HCl (100 mL). After stirring for 30 min, the reaction mixture was then poured into ice-water and extracted with EtOAc. The combined extracts were concentrated, dried over anhydrous MgSO4, filtered and concentrated in vacuo. The material was dissolved in THF and added dropwise to a stirred solution of NH4OH (17 mL) in THF (17 mL) at 5° C. After stirring 30 min, the mixture was concentrated under reduced pressure and extracted with EtOAc. The combined extracts were washed with H2O, dried over anhyd MgSO4, concentrated and purified by column chromatography (Hex/EtOAc=5:1) to afford 2-chloro-6-fluoro-4-sulfamoylbenzyl acetate (1.02 g, 15%, 3 steps) as an orange solid. 1H NMR (400 MHz, CDCl3) δ 7.80 (t, 1H), 7.59 (dd, 1H), 5.28 (d, 2H), 5.16 (s, 2H), 2.10 (d, 3H); MS (EI) m/z 303 (M+Na+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846739B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-b356df047f9447be9511302b2c54977f |
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| Source note | uspto-grants-2014_09 |
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