Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957695Generated: November 3, 2026

Tetrahydrofuran → Allyl 4-[3-(1-adamantyl)-4-methoxyethoxymethoxybenzamido]benzoate

https://huagongshe.com/reaction/1957695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
ReactantProp-2-en-1-yl 4-aminobenzoateHCID 13075143—
Reactant3-(1-Adamantyl)-4-methoxyethoxymethoxybenzoyl chlorideHCID 57233102—
SolventWaterHCID 962—
ProductAllyl 4-[3-(1-adamantyl)-4-methoxyethoxymethoxybenzamido]benzoateHCID 67663874—

Reaction Steps

700 mg (3.95 mmol) of allyl 4-aminobenzoate, 1 ml (4.3 mmol) of triethylamine and 50 ml of THF were introduced into a round-bottomed flask. A solution of 1.5 g (3.96 mmol) of 3-(1-adamantyl)-4-methoxyethoxymethoxybenzoyl chloride was added dropwise and the mixture was stirred at room temperature for 4 hours. The reaction medium was poured into water and extracted with ethyl ether. The organic phase was separated out after settling had taken place, dried over magnesium sulfate and evaporated. The residue obtained was purified by chromatography on a column of silica, eluted with dichloromethane. 1.7 g (83%) of the expected allylic ester was recovered in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05786379
Source datasetuspto-grants-1998_07
ORD IDord-b46855fa87a44f10b58563b1917e71b5
Source noteuspto-grants-1998_07