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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 713829Generated: October 30, 2026

Tetrahydrofuran → Gamma-Butyrolactone

https://huagongshe.com/reaction/713829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantDimethyl maleateHCID 5271565—
ReactantHCID 178418361HCID 178418361—
SolventWaterHCID 962—
ProductGamma-ButyrolactoneHCID 7302—
Product1,4-ButanediolHCID 8064—

Reaction Steps

The dialkyl maleate produced in the second esterification stage 13 is fed to a hydrogenation stage 17. For the hydrogenation, hydrogen 19 is also introduced into the hydrogenation stage 17. In the hydrogenation stage 17, the dimethyl maleate is reacted with the hydrogen to form tetrahydrofuran and optionally 1,4-butanediol and/or γ-butyrolactone with simultaneous formation of alkanol and water, as described, for example, in WO 88/00937, WO 91/01960, WO 03/006446 or WO 05/058855. The alkanol formed in the hydrogenation is the same alkanol as that which was introduced in the first esterification stage 9 and second esterification stage 13.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09186599B2
Source datasetuspto-grants-2015_11
ORD IDord-4bda3faa2a3f4f4fa952f63e78a6a6fc
Source noteuspto-grants-2015_11