HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795889Generated: November 2, 2026
Water → 4-Dimethylthiocarbamoyloxy-2,3-difluoro-5-nitrobenzoic acid methyl ester
https://huagongshe.com/reaction/1795889
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Dimethylthiocarbamoyl chloride | HCID 27871 | — |
| Reactant | HCID 22180109 | HCID 22180109 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Dimethylthiocarbamoyloxy-2,3-difluoro-5-nitrobenzoic acid methyl ester | HCID 54233431 | — |
Reaction Steps
A solution of methyl 2,3-difluoro-4-hydroxy-5-nitrobenzoate in N,N-dimethylformamide is treated with one molar equivalent of cesium carbonate and warmed to 85° C. for 30 minutes. The stirring mixture is then treated dropwise rapidly with a solution comprised of a slight excess of N,N-dimethylthiocarbamoyl chloride in N,N-dimethylformamide. The reaction mixture is stirred at room temperature for one hour, or may be warmed over a steam bath for one hour. The mixture is then poured into water and extracted with ethyl acetate. The organic phase is washed with 5% aqueous sodium hydroxide, water, and brine, and is then dried with a drying agent like magnesium sulfate of sodium sulfate. The solvent is then removed in vacuo to give a crude product. The compound is purified by ordinary methods such as chromatography or crystallization from an appropriate solvent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07030119B1 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-2f58cdf9bd5248d2b815d73fd71f3935 |
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| Source note | uspto-grants-2006_04 |
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