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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 438022Generated: October 30, 2026

Benzyl Alcohol → HCID 53990429, compound

https://huagongshe.com/reaction/438022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantCarbon DioxideHCID 280—
ReactantHCID 68122688HCID 68122688—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53990429HCID 53990429—

Reaction Steps

A mixture of 10.4 g (0.027 mole) of 2-(5-tetradecyloxy)thenoylacetic acid, 4.4 g (0.027 mole) of N,N'-carbonyldiimidazole, and anhydrous tetrahydrofuran is stirred until the evolution of carbon dioxide gas stops. The mixture is cooled on an ice bath, in 3.0 g (0.027 mole) of benzyl alcohol is added. The reaction is allowed to warm to room temperature and evaporated to dryness. The residue is extracted with ether-H2O. The ether layer is washed with 10% aqueous HCl, then water, then saturated sodium chloride, dried with sodium sulfate and evaporated to dryness to give 5-tetradecyloxythen-2-oylacetic acid benzyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04032647
Source datasetuspto-grants-1977_06
ORD IDord-9b4f6c6476ea46b1be1fa39eb534d584
Source noteuspto-grants-1977_06