HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544432Generated: October 30, 2026
Hydrochloric Acid → HCID 57116472, compound
https://huagongshe.com/reaction/544432
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | (2-Phenoxy-5-thiazolyl)-methanol | HCID 13106154 | — |
| Reactant | (1R,3S) 2,2-dimethyl-3[(dihydro-2-oxo-3-(2H)-thienylidene)-methyl]-cyclopropane-1-carboxylic acid chloride | HCID 88716027 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 57116472 | HCID 57116472 | 43.4% |
Reaction Steps
2.1 g of (2-phenoxy-5-thiazolyl)-methanol were added to a solution of 2.44 g of (1R,3S) 2,2-dimethyl-3[(dihydro-2-oxo-3-(2H)-thienylidene)-methyl]-cyclopropane-1-carboxylic acid chloride [described in French Pat. No. 70-21682] in 50 ml of benzene and 3 ml of pyridine were added thereto dropwise at 0° C. The mixture was stirred at 20° C. for 24 hours and was then poured into aqueous 2N hydrochloric acid solution. The decanted organic phase was dried and evaporated to dryness under reduced pressure. The residue was chromatographed over silica gel and was eluted with benzene. The product was crystallized from ethyl acetate to obtain 1.8 g of (2-phenoxy-5-thiazolyl)-methyl (1R,3S) 2,2-dimethyl-3-[(dihydro-2-oxo-3-(2H)-thienylidene)-methyl]-cyclopropane-1-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04450169 |
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| Source dataset | uspto-grants-1984_05 |
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| ORD ID | ord-cc7596375e234cd5808f46107f45c232 |
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| Source note | uspto-grants-1984_05 |
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