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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129663Generated: October 26, 2026

Water → Allyl 4-[3-(1-adamantyl)-4-methoxybenzoyloxy-]2-fluorobenzoate

https://huagongshe.com/reaction/129663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant3-(1-Adamantyl)-4-methoxybenzoyl chlorideHCID 10804497—
ReactantAllyl 2-fluoro-4-hydroxybenzoateHCID 14852522—
SolventTetrahydrofuranHCID 8028—
ProductAllyl 4-[3-(1-adamantyl)-4-methoxybenzoyloxy-]2-fluorobenzoateHCID 1485248978.1%

Reaction Steps

To a mixture of 1.96 g (10 mmoles) of allyl 2-fluoro-4-hydroxybenzoate, 1.53 ml (11 mmoles) of triethylamine and 25 ml of THF, there is slowly added a solution of 3 g (10 mmoles) of 3-(1-adamantyl)-4-methoxybenzoyl chloride in 50 ml of THF. The reaction medium is stirred at ambient temperature for 12 hours and then poured into water and extracted with ethyl ether. The organic phase is decanted, washed with water, dried on magnesium sulfate and evaporated. The resulting residue is purified by chromatography on a silica column, eluted by a 50:50 mixture of dichloromethane and hexane. After evaporation of the solvents, 3.63 g (78% yield) of the expected ester having a melting point of 102°-104° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05468897
Source datasetuspto-grants-1995_11
ORD IDord-d3a2396790a547aa89c7fa67fe94cbfc
Source noteuspto-grants-1995_11