Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234492Generated: October 25, 2026

Pyridine → 1,1-Dimethylethyl 4-methylbenzoate

https://huagongshe.com/reaction/234492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactanttert-ButanolHCID 6386—
Reactant4-Methylbenzoyl ChlorideHCID 13405—
SolventWaterHCID 962—
Product1,1-Dimethylethyl 4-methylbenzoateHCID 1162974980.1%

Reaction Steps

37 g of tert-butanol and then 26 ml of pyridine are added to 39.04 g of p-toluoyl chloride and the reaction mixture is refluxed for 3 hours. After cooling, it is poured into water, extracted with AcOEt, washed with a 1N solution of HCl and then with a 5% solution of sodium hydrogencarbonate, dried over sodium sulfate and evaporated under vacuum. The residue is chromatographed on silica using hexane and then a hexane/DCM mixture (80/20; v/v) as the eluent to give 38.9 g of the expected product, which is used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594023
Source datasetuspto-grants-1997_01
ORD IDord-322a45395b44461bbbe7c7c16a2bbff1
Source noteuspto-grants-1997_01