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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 246809Generated: October 29, 2026

Benzoyl chloride → HCID 54148715, compound

https://huagongshe.com/reaction/246809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
Reactant4-MethylpyridineHCID 7963—
ReactantHCID 136010418HCID 136010418—
SolventDichloromethaneHCID 6344—
ProductHCID 54148715HCID 5414871580%

Reaction Steps

Benzoyl chloride (0.12 g) and 4-methylpyridine (0.08 g) were added dropwise with stirring to a solution of 2-[1-(ethoxyimino)butyl]-5-(4,5-dimethyl-2-thiazolyl)-3-hydroxycyclohex-2-en-1-one (2) (0.27 g) in dichloromethane (40 ml) at ambient temperature. After 1 hour the solution was washed with cold dilute aqueous sodium hydroxide, followed by cold dilute hydrochloric acid and then dried over magnesium sulphate and evaporated to give 2-[1-(ethoxyimino)butyl]-3-benzoyloxy-5-(4,5-dimethyl-2-thiazolyl)cyclohex-2-en-1-one (0.28 g, 80%) as an orange oil. The product was characterized by proton nuclear magnetic resonance spectroscopy and appropriate physical data are recorded in Example 5 Table 6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04704157
Source datasetuspto-grants-1987_11
ORD IDord-b48302bbe0ba47c5bbd758275bff5ac9
Source noteuspto-grants-1987_11