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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275060Generated: October 26, 2026

Triethyl Citrate → Ethyl tetrahydrofurfurylacetate

https://huagongshe.com/reaction/275060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl CitrateHCID 6506—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 178418361HCID 178418361—
ProductEthyl tetrahydrofurfurylacetateHCID 26317539%
Product2-(Oxolan-3-yl)ethan-1-olHCID 1112622530%

Reaction Steps

400 ml of triethyl citrate were hydrogenated at 175° C. and 50 bar together with 1100 ml of tetrahydrofuran and 60 g of catalyst F (4-mm tablets) until the take-up of hydrogen had ceased. The reaction product was freed from tetrahydrofuran and distilled under reduced pressure, giving 101 g (39%) of ethyl tetrahydrofurfurylacetate and 57 g (30%) of 3-(2'-hydroxyethyl)tetrahydrofuran.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05391771
Source datasetuspto-grants-1995_02
ORD IDord-b5ff5c4a485e45258089b7c7e10d1743
Source noteuspto-grants-1995_02