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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086391Generated: November 2, 2026

Ethanol → Succinate

https://huagongshe.com/reaction/1086391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTetrahydrofuranHCID 8028—
ReactantDiethylstilbestrolHCID 448537—
ReactantDiethyl MaleateHCID 5271566—
Solvent1-ButanolHCID 263—
SolventWaterHCID 962—
ProductSuccinateHCID 160419—
ProductDiethyl MaleateHCID 5271566—
ProductFumarateHCID 5460307—

Reaction Steps

EP-A 255,400 describes a method of producing pure GBL whereby the problem of the azeotrope formed by GBL and DES is avoided by adding diethyl maleate. The mixture of BD, THF, GBL, DES, ethanol, n-butanol and water produced by catalytic hydrogenation of diethyl maleate, fumarate or succinate is distilled in a first column such that ethanol, water, THF and n-butanol are removed at the top, whilst all other components remain at the bottom of the column. The bottoms from the first column are then distilled in a second column such that the GBL/DES azeotrope is removed at the top and the BD remains at the bottom. Purification of the GBL is effected by passing the overheads from the second column to a third column together with a suitable amount of diethyl maleate as used as starting material for the catalytic hydrogenation. Pure GBL is removed at the top of the column.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05030328
Source datasetuspto-grants-1991_07
ORD IDord-2a8e42a38db040c685f30bf1951127de
Source noteuspto-grants-1991_07