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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1109953Generated: October 25, 2026

Diethyl Ether → 4-[(S)-2-methylbutoxycarbonyl]phenyl 4-[(S)-2-propoxypropanoyloxy]benzoate

https://huagongshe.com/reaction/1109953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantBenzoic acid, 4-hydroxy-, (2S)-2-methylbutyl esterHCID 13530950—
Reactant4-[(S)-2-Propoxypropanoyloxy]benzoic acidHCID 14793534—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product4-[(S)-2-methylbutoxycarbonyl]phenyl 4-[(S)-2-propoxypropanoyloxy]benzoateHCID 1484878774.1%

Reaction Steps

In 12 ml of methylene chloride were dissolved 107 mg of 4-[2-(S)-propoxypropanoyloxy]benzoic acid, 95 mg of 4-[(S)-2-methyl butoxycarbonyl]phenol, and 140 mg of dicyclohexylcarbodiimide, and a catalytic amount of 4-dimethylaminopyridine was added to the solution, followed by stirring at room temperature. After 5 hours, diethyl ether was added to the reaction mixture, and any insoluble matter was removed by filtration. The filtrate was washed successively with a 10% hydrochloric acid aqueous solution, a saturated sodium bicarbonate aqueous solution, water, and a saturated sodium chloride aqueous solution, and dried over sodium sulfate. The solvent was removed from the residue by distillation, and the resulting oily substance was purified by silica gel column chromatography to obtain 139 mg of the entitled compound as a transparent oily substance. This compound did not crystalize even when allowed to stand at room temperature or less for a long time. The structure of the compound was confirmed by NMR and IR spectra.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05324451
Source datasetuspto-grants-1994_06
ORD IDord-4b8bae25343c46f4b7223d4db5d4d0e0
Source noteuspto-grants-1994_06