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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544436Generated: October 31, 2026

Hydrochloric Acid → HCID 57288734, compound

https://huagongshe.com/reaction/544436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(2-Phenoxy-5-thiazolyl)-methanolHCID 13106154—
ReactantHCID 88716184HCID 88716184—
SolventBenzeneHCID 241—
SolventPyridineHCID 1049—
ProductHCID 57288734HCID 57288734—

Reaction Conditions

Temperature20 °C

Reaction Steps

2 g of (2-phenoxy-5-thiazolyl)-methanol were added to a solution of (1R,3R)2,2-dimethyl-3-[(dihydro-2-oxo-3-(2H)-thienylidene)-methyl]-cyclopropane-1-carboxylic acid chloride [described in French Pat. No. 70-21682 published under No. 2.097.244] prepared from 2.2 g of the corresponding acid in 30 ml of benzene and 0.81 ml of pyridine were added thereto at -10° C.The reaction mixture was stirred at 20° C. for 17 hours and was poured into aqueous dilute hydrochloric acid. The decanted aqueous phase was extracted with ether and the combined organic phases were washed with water, dried and evaporated to dryness under reduced pressure. The residuewas chromatographed over silica gel and was eluted with an 8-2 cyclohexane-ethyl acetate mixture to obtain 2.9 g of (2-phenoxy-5-thiazolyl)-methyl (1R,3R) 2,2-dimethyl-3[(dihydro-2-oxo-3-(2H)-thienylidene)-methyl]-cyclopropane-1-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04450169
Source datasetuspto-grants-1984_05
ORD IDord-003be50959e544faa25abbbabcf9be27
Source noteuspto-grants-1984_05