HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343012Generated: October 30, 2026
Dimethyl Disulfide → HCID 10058722, compound
https://huagongshe.com/reaction/343012
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Disulfide | HCID 12232 | — |
| Reactant | 3,4-Difluorobenzoic acid | HCID 99166 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10058722 | HCID 10058722 | 83.1% |
Reaction Steps
n-Butyllithium (2.5 m in hexane, 35 ml) was added with cooling to a solution of 3,4-difluorobenzoic acid (5.5 g) in dry tetrahydrofuran while maintaining the temperature below -70° C. The mixture was stirred for 2 hours at -70° C. A solution of dimethyl disulphide (19.8 g) in tetrahydrofuran was added and the mixture was stirred at -70° C. for 1.5 hours. It was allowed to warm to room temperature, diluted with ether and washed with water. The aqueous layer was acidified to pH 1 and extracted with ether, washed with water, dried (anhydrous MgSO4) and filtered. The filtrate was evaporated to dryness and the residue was recrystallised from a mixture of cyclohexane and ether to give 3,4-difluoro-2-(methylsulphenyl)benzoic acid (5.9 g) as a white solid, m.p. 149.2°-149.6° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05859283 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-651a8d98ab1d40dda5b476e996a0d25a |
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| Source note | uspto-grants-1999_01 |
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