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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388640Generated: October 31, 2026

Pyridine → HCID 54121726, compound

https://huagongshe.com/reaction/1388640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
ReactantHCID 136017126HCID 136017126—
SolventDichloromethaneHCID 6344—
ProductHCID 54121726HCID 54121726—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a reaction mixture containing 3.6 gms (0.01 mol) of 2-{1-[(5-chlorothien-2-ylmethoxy)imino]butyl}-3-hydroxy-5,5-dimethylcyclohex-2-en-1-one and 0.87 gm (0.011 mol) of pyridine in 20 mls of methylene chloride stirred at 0° C. is added 0.89 gm (0.011 mol) of acetyl chloride. The mixture is then stirred at room temperature for 2 hours. The mixture is then worked up by washing with water, drying with anhydrous magnesium sulfate, and filtered. The filtrate is evaporated under vacuum affording 3-acetyloxy-2-{1-[(5-chlorothien-2-ylmethoxy)imino]butyl}-5,5-dimethylcyclohex-2-en-1-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04432786
Source datasetuspto-grants-1984_02
ORD IDord-8ea386af31c74eb9a81e06f0dfdcb941
Source noteuspto-grants-1984_02