Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390373Generated: November 1, 2026

Methylparaben → HCID 60778955, compound

https://huagongshe.com/reaction/390373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylparabenHCID 7456—
ReactantTriphenylphosphineHCID 11776—
ReactantSodium HydroxideHCID 14798—
ReactantTetrahydro-3-furanmethanolHCID 139980—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 60778955HCID 6077895548.3%

Reaction Steps

To a solution of tetrahydrofuran-3-ylmethanol (21.89 g), methyl 4-hydroxybenzoate (33.5 g) and triphenylphosphine (64.5 g) in tetrahydrofuran (400 ml) was slowly added dropwise a solution of diethyl azodicarboxylate in toluene (120 mL, 40% toluene solution) at 0° C., and the mixture was stirred at room temperature for 2 hr. The reaction solution was concentrated, triphenylphosphine oxide was precipitated from ethyl acetate-hexane and removed by filtration with a glass filter, and the mother liquor was concentrated. The residue was purified by silica gel column chromatography [developing solvent; hexane:ethyl acetate=90:10 (volume ratio)-*hexane:ethyl acetate=40:10 (volume ratio)] to give a colorless oil. The obtained colorless oil was dissolved in tetrahydrofuran (200 mL) and methanol (100 mL), 8N aqueous sodium hydroxide solution (100 mL) was added, and the mixture was stirred at 80° C. for 2 hr with heating. The reaction solution was concentrated, cooled to 0° C., neutralized with 6N hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to give the title compound (23 g, yield 48%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383647B2
Source datasetuspto-grants-2013_02
ORD IDord-b0dc01a8a09344759effe9472df36e17
Source noteuspto-grants-2013_02