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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293544Generated: October 30, 2026

Cyclohexanol → HCID 21476982, compound

https://huagongshe.com/reaction/2293544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanolHCID 7966—
ReactantTriphenylphosphineHCID 11776—
ReactantMethyl 2,4-DihydroxybenzoateHCID 16523—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21476982HCID 21476982—

Reaction Steps

A 3.00 g portion of methyl 2,4-dihydroxybenzoate was dissolved in 30 ml of tetrahydrofuran, and 2 ml of cyclohexanol, 9.00 g of triphenylphosphine and 7.38 ml of diisopropyl azodicarboxylate were added, followed by stirring for 12 hours at room temperature. After completion of the reaction, the solvent was evaporated, the resulting residue was mixed with hexane-ethyl acetate, and insoluble matter was removed by filtration. Solvent of the filtrate was evaporated and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=12:1-2:1) to give 1.70 g of methyl 4-cyclohexyloxy-2-hydroxybenzoate. Nuclear magnetic resonance spectrum (DMSO-d6, TMS internal standard) δ: 1.10-2.10 (10H, m), 3.86 (3H, s), 4.40-4.48 (1H, m), 6.43-6.58 (2H, m), 7.63-7.75 (1H, m), 10.71 (1H, s)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05686482
Source datasetuspto-grants-1997_11
ORD IDord-a3739f55996f4d4ea98a0c8e213f4e58
Source noteuspto-grants-1997_11