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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324156Generated: October 31, 2026

Dicyclohexylcarbodiimide → (S)-4-[4'-(2''-methylbutylcarbonyloxy)phenyl]-1-benzyloxybenzene

https://huagongshe.com/reaction/324156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant(S)-3-methyl-pentanoic acidHCID 642230—
Reactant4-(4-Benzyloxyphenyl)phenolHCID 15268847—
SolventDichloromethaneHCID 6344—
Product(S)-4-[4'-(2''-methylbutylcarbonyloxy)phenyl]-1-benzyloxybenzeneHCID 2064578292.2%

Reaction Steps

{circle around (1)}: A mixture comprising 2.8 g of 4-(4′-benzyloxyphenyl)phenol, 1.2 g of (S)-2-methylbutylcarboxylic acid, 3.09 g of DCC and 15 g of dichloromethane was stirred at room temperature for 30 minutes. Then, a catalytic amount of 4-N,N-dimethylaminopyridine was added to the mixture, and the mixture was further stirred at room temperature for 12 hours. After finishing the reaction, insoluble substances were filtered off, followed by distilling off dichloromethane from the filtrate. The resultant residue was purified by means of silica gel column chromatography, whereby 3.5 g of (S)-4-[4′-(2″-methylbutylcarbonyloxy)phenyl]-1-benzyloxybenzene was obtained in the form of a colorless crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06217793B1
Source datasetuspto-grants-2001_04
ORD IDord-f7f6de8ed2ec4105a7df70badad5e3ab
Source noteuspto-grants-2001_04