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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129668Generated: October 26, 2026

Water → Methyl 4-[3-(1-adamantyl)-4-methoxybenzoyloxy]-2-hydroxybenzoate

https://huagongshe.com/reaction/129668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethyl 2,4-DihydroxybenzoateHCID 16523—
Reactant3-(1-Adamantyl)-4-methoxybenzoyl chlorideHCID 10804497—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-[3-(1-adamantyl)-4-methoxybenzoyloxy]-2-hydroxybenzoateHCID 1485250059%

Reaction Steps

Into a round bottom flask, there are introduced 1.68 g (10 mmoles) of methyl 2,4-dihydroxybenzoate, 1.55 ml (11 moles) of triethylamine and 50 ml of THF. There is then slowly added a solution of 3 g (10 mmoles) of 3-(1-adamantyl)-4-methoxybenzoyl chloride in 50 ml of THF and the mixture is stirred at ambient temperature for 12 hours. The reaction medium is 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, 2.55 g (59% yield) of methyl 4-[3-(1-adamantyl)-4-methoxybenzoyloxy]-2-hydroxybenzoate having a melting point of 125°-127° C. are recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05468897
Source datasetuspto-grants-1995_11
ORD IDord-85f2b8ff014f419fa53d639c332b1ee8
Source noteuspto-grants-1995_11