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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975825Generated: November 1, 2026

Hydrochloric Acid → Scopine-2,2-dithienyl glycolate

https://huagongshe.com/reaction/975825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(1α,2β,4β,5α)-9-Methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7α-olHCID 1274465—
ReactantSodiumHCID 5360545—
ReactantMethyl alpha-hydroxy-alpha-2-thienyl-2-thiopheneacetateHCID 11414137—
SolventTolueneHCID 1140—
ProductScopine-2,2-dithienyl glycolateHCID 29927228—

Reaction Conditions

Temperature90 °C

Reaction Steps

38.15 g (0.15 mole) of methyl di-(2-thienyl)glycolate and 23.28 g (0.15 mole) of scopine are mixed, 0.34 g (0.015 gram atom) of sodium is added and the mixture is melted in a heating bath at 90° C. under a water jet vacuum. The reaction lasts 2.5 hours. 100 ml of absolute toluene are then added and the mixture is stirred at a heating bath temperature of 90° C. until a solution is produced. The reaction solution is cooled to room temperature and stirred into a mixture of ice and hydrochloric acid cooled using ice. The hydrochloride of the basic ester crystallising out is filtered off under suction and washed using a small amount of water and a large amount of diethyl ether. The filtrate phases are separated off and the aqueous phase is extracted using diethyl ether. The hydrochloride filtered off under suction is suspended in the (acid) aqueous phase and converted to the base while monitoring the temperature and adding the corresponding amount of sodium carbonate; the base is extracted using methylene chloride. The combined methylene chloride phases are dried over sodium sulphate. After distilling off the methylene chloride, crystals remain which are purified over active charcoal and recrystallised from acetonitrile. Pale yellow crystals (from acetonitrile), m.p. 148°-49° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05610163
Source datasetuspto-grants-1997_03
ORD IDord-cc6fc777ac7944c29a0902a19bcc9718
Source noteuspto-grants-1997_03