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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604635Generated: November 1, 2026

ethyl (E)-3-[2-(4-tert-butylthiazol-2-yl)benzofuran-5-yl]propenoate → Ethyl 3-[2-(4-tert-butylthiazol-2-yl)benzofuran-5-yl]propionate

https://huagongshe.com/reaction/1604635

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl (E)-3-[2-(4-tert-butylthiazol-2-yl)benzofuran-5-yl]propenoateHCID 86754881—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-[2-(4-tert-butylthiazol-2-yl)benzofuran-5-yl]propionateHCID 1960366299.4%

Reaction Steps

A solution of ethyl (E)-3-[2-(4-tert-butylthiazol-2-yl)-benzofuran-5-yl-]propenoate (0.65 g) in tetrahydrofuran (10 ml) was hydrogenated over 10% Pd--C (0.1 g) at room temperature under atmospheric pressure. After removal of the catalyst by filtration the filtrate was concentrated under reduced pressure to give ethyl 3-[2-(4-tert-butylthiazol-2-yl)benzofuran-5-yl]propionate (0.65 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994378
Source datasetuspto-grants-1999_11
ORD IDord-bbfc218121b8439385134455d9d025d2
Source noteuspto-grants-1999_11