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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369683Generated: October 28, 2026

Benzoyl chloride → 4-Benzyloxy-3-ethyl-5-methylphenyl benzoate

https://huagongshe.com/reaction/369683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant3-Ethyl-4-benzyloxy-5-methylphenolHCID 22006725—
SolventChloroformHCID 6212—
Product4-Benzyloxy-3-ethyl-5-methylphenyl benzoateHCID 5423609693.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 6.3 g of 4-benzyloxy-3-ethyl-5-methylphenol, 3.2 g of triethylamine and 50 ml of chloroform was added dropwise 4.0 g of benzoyl chloride with stirring at 0° C. After stirring at room temperature for 6 hours, the reaction mixture was concentrated under reduced pressure. To the residue was added 100 ml of 10% hydrochloric acid, which was extracted with 100 ml of ethyl acetate. The ethyl acetate layer was washed with 10% hydrochloric acid, aqueous sodium hydrogencarbonate solution and then saturated sodium chloride solution, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure, which afforded 8.4 g of crude 4-benzyloxy-3-ethyl-5-methylphenyl benzoate (yield, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140274
Source datasetuspto-grants-2000_10
ORD IDord-3bd233dbe9904109b7a81ed38e5f9117
Source noteuspto-grants-2000_10