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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248002Generated: October 25, 2026

Pyridine → Phenyl [4-(tetradecyloxy)phenyl]methyl carbonate

https://huagongshe.com/reaction/248002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenyl chloroformateHCID 15891—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Tetradecyloxybenzyl alcoholHCID 10087384—
SolventDichloromethaneHCID 6344—
ProductPhenyl [4-(tetradecyloxy)phenyl]methyl carbonateHCID 10411003—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. mixture of 9.0 g of product from Example 19, 4.44 g of pyridine and 70 ml of methylene chloride is added, dropwise, 5.28 of phenyl chloroformate. The reaction is stirred at 0° C. for 15 minutes; followed by room temperature for 30 minutes. The mixture is poured into saturated sodium bicarbonate and the aqueous layer is extracted with methylene chloride. The combined organic layers are washed with saturated sodium chloride, dried and concentrated in vacuo. The residue is purified by column chromatography (silica gel: 0-5% ethyl acetate/hexane) to give 12.6 g of colorless prisms.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05208247
Source datasetuspto-grants-1993_05
ORD IDord-f74921ea5ccd4e1e8f1a6b2340757ce0
Source noteuspto-grants-1993_05