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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442439Generated: October 29, 2026

Hydrochloric Acid → Ethyl 7-[3,4-dihydroxy-2-(3-hydroxyoctyl)cyclopentyl]heptanoate

https://huagongshe.com/reaction/442439

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl 7-{3,4-di(2-tetrahydropyranyloxy)2-[3-(2-tetrahydropyranyloxy)octyl]cyclopentyl}heptanoateHCID 20354841—
SolventEthanolHCID 702—
ProductEthyl 7-[3,4-dihydroxy-2-(3-hydroxyoctyl)cyclopentyl]heptanoateHCID 2035485796.2%

Reaction Steps

A mixture of ethyl 7-{3,4-di(2-tetrahydropyranyloxy)-2-[3-(2-tetrahydropyranyloxy)octyl]cyclopentyl}heptanoate (5.5 g.) [prepared as described in (o) above], ethanol (100 ml.), N hydrochloric acid (100 ml.) and a cation-exchange resin [Dowex resin AG50W-X 8H+ (7.5 g.)] was stirred at 50°-60° C. for 18 hours. The mixture was then cooled and filtered and the solid washed with diethyl ether and water. The combined filtrate and washings were evaporated in vacuo to remove organic solvents and the aqueous residue extracted with diethyl ether. The ethereal extract was dried over anhydrous sodium carbonate and evaporated in vacuo to give ethyl 7-[3,4-dihydroxy-2-(3-hydroxyoctyl)cyclopentyl]heptanoate (3.2 g.), which was used as starting material in the following preparation (q) of 7-[3,4-dihydroxy-2-(3-hydroxyoctyl)cyclopentyl]heptanoic acid without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04045467
Source datasetuspto-grants-1977_08
ORD IDord-13579c8008d147788e11c5e100e6c8ad
Source noteuspto-grants-1977_08