HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789574Generated: October 30, 2026
Sulfur Dioxide → Lithium 3-chloro-4-ethoxycarbonyl-1-methylpyrazole-5-sulfinate
https://huagongshe.com/reaction/1789574
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | Ethyl 3-chloro-1-methyl-1H-pyrazole-4-carboxylate | HCID 13687029 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Lithium 3-chloro-4-ethoxycarbonyl-1-methylpyrazole-5-sulfinate | HCID 23704643 | — |
Reaction Steps
5.0 g of ethyl 3-chloro-1-methylpyrazole-4-carboxylate was dispersed in dry diethyl ether under cooling at -60° C. or lower. Into this solution there was added lithium diisopropylamide (1.2 molar equivalent) and after stirring for an hour sulfur dioxide gas was passed into this solution for 30 minutes. After stirring at -60° C. for 2 hours the reaction mixture was stirred at room temperature for 2 hours. Filtration and drying of the precipitate gave 6.0 g of lithium 3-chloro-4-ethoxycarbonyl-1-methylpyrazole-5-sulfinate. This product was added into a solution of 100 ml of ice-water and 100 ml of dichloromethane and 6.0 g of N-chloro succinimide was added thereinto at 0°-5° C. After stirring for 45 minutes at room temperature the dichloromethane layer was separated and water layer was extracted with 100 ml of dichloromethane. The combined dichloromethane solution of 3-chloro-4-ethoxycarbonyl-1-methylpyrazole-5-sulfonyl chloride (b.p.: 133° C./ 0.25 mmHg.) was added dropwise into 80 ml of aqueous ammonia (28%) under cooling at 10° C. After stirring for an hour, evaporation of the solvent gave 3.6 g of 3-chloro-4-ethoxycarbonyl-1-methylpyrazole-5-sulfonamide. m.p.: 121°-123° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04689417 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-e765de5f47654addb30791e3c03fffd2 |
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| Source note | uspto-grants-1987_08 |
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