HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329604Generated: October 29, 2026
Potassium Carbonate → HCID 13747728, compound
https://huagongshe.com/reaction/329604
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Vinyl chloroformate | HCID 78808 | — |
| Reactant | HCID 13747806 | HCID 13747806 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 13747728 | HCID 13747728 | — |
Reaction Steps
5.5 g 4-(4-(1,1-dimethylethyl)-2-thiazolyl)-1-phenylmethyl-1,2,3,6-tetrahydropyridine, 2.5 g K2CO3 and 50 ml 1,2-dichloroethane are treated dropwise at -10° to -7° under stirring with 3.75 ml chloroformic acid vinyl ester. The mixture is stirred at -10° to -7° for 3 hours. The solvent is evaporated, the residue partitioned between water and hexane. and the water phase extracted with hexane. The combined organic layers are washed with saturated brine solution, filtered and dried (Na2SO4). The solvent is evaporated and the oily residue is added under ice-cooling to 20% aqueous hydrochloric acid. The mixture is heated on a steam bath for 4 hours, then cooled to room temperature and extracted once with dichloromethane.The aqueous acidic solution is filtered, made alkaline with aqueous NaOH and extracted with ethyl ether. After evaporation of ether, the heading compound is obtained as an oily residue. M.p. of the hydrogenmaleinate is 170°-171°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04892879 |
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| Source dataset | uspto-grants-1990_01 |
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| ORD ID | ord-dfbbb2c550204045b4c8054dd491c472 |
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| Source note | uspto-grants-1990_01 |
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