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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091164Generated: November 3, 2026

Pyridine → HCID 19761580, compound

https://huagongshe.com/reaction/1091164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetyl chlorideHCID 6367—
ReactantBenzenemethanol, 4-ethenyl-α,α-dimethyl-HCID 12542438—
SolventDichloromethaneHCID 6344—
ProductHCID 19761580HCID 1976158048%

Reaction Steps

A mixture of 6.7 g of 1-(1-hydroxy-1-methylethyl)-4-ethenyl-benzene and 4.0 g of pyridine in 100 ml of dichloromethane was stirred while 4.0 g of acetyl chloride in 20 ml of dichloromethane was added dropwise. After the addition was complete, the mixture was refluxed gently overnight. After cooling, an additional 30 ml of dichloromethane was added and the mixture was then washed with 50 ml of cold 5% aqueous HCl, and then several times with 30 ml portions of water. After drying over magnesium sulfate, filtering, and concentrating, the crude product was purified by HPLC using ethyl/acetate hexane as eluent. This method affords 4.05 g (47.5% yield) of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05084522
Source datasetuspto-grants-1992_01
ORD IDord-77e3af6566764a2581382900c2af2512
Source noteuspto-grants-1992_01