HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369580Generated: October 27, 2026
Water → 2-Chloro-4-methylsulfonyl-3-(3-oxetanyloxy)benzoic acid
https://huagongshe.com/reaction/369580
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Oxetan-3-ol | HCID 9942117 | — |
| Reactant | 2-Chloro-3-fluoro-4-methylsulfonylbenzoic acid | HCID 15451759 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Chloro-4-methylsulfonyl-3-(3-oxetanyloxy)benzoic acid | HCID 23282342 | 57.5% |
Reaction Steps
A mixture of 0.76 g (19 mmol) of 60 percent in mineral oil sodium hydride in dry N,N-dimethylformamide was prepared in a flask under a nitrogen blanket and to it was added 2.02 g (8.0 mmol) of 2-chloro-3-fluoro-4-methylsulfonylbenzoic acid in portions with stirring at ambient temperature. The mixture was allowed to cool and then 0.71 g (9.6 mmol) of 3-hydroxyoxetane was added dropwise with stirring. There was an exotherm. After one hour, the reaction appeared to be complete and water was added cautiously. The resulting aqueous solution was extracted with ether and was then acidified with 1N aqueous hydrochloric acid. The resulting mixture was extracted three times with ethyl acetate and the three extracts were combined, washed with water, dried over magnesium sulfate, and concentrated by evaporation under reduced pressure. The residue was crystallized with a mixture of acetone and hexane to obtain 1.41 g of the title compound as white crystals melting at 180-183° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06140271 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-258ff3e9bbf443ca949c60f4bd5e4bcc |
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| Source note | uspto-grants-2000_10 |
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