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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799109Generated: October 26, 2026

Ethyl 5-(3-methoxyprop-1-ynyl)-2-phenylthiazole-4-carboxylate → Ethyl 5-(3-methoxypropyl)-2-phenylthiazole-4-carboxylate

https://huagongshe.com/reaction/1799109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-(3-methoxyprop-1-ynyl)-2-phenylthiazole-4-carboxylateHCID 67425118—
SolventEthyl AcetateHCID 8857—
ProductEthyl 5-(3-methoxypropyl)-2-phenylthiazole-4-carboxylateHCID 6742511988%

Reaction Steps

Ethyl 5-(3-methoxyprop-1-ynyl)-2-phenylthiazole-4-carboxylate (26.1 g, 86.6 mmol) was dissolved in EtOAc (350 mL) and hydrogenated under balloon pressure for four days until LCMS indicated complete reduction of unsaturation. On day three, the catalyst was removed by filtration, fresh catalyst added and the mixtures re-subjected to hydrogenation at balloon pressure. The catalyst was removed by filtration through a pad of celite. The filter pad was rinsed with EtOAc and the filtrate concentrated to dryness. The crude product was purified by MPLC eluting with pentane/EtOAc to give ethyl 5-(3-methoxypropyl)-2-phenylthiazole-4-carboxylate (23.2 g, 88% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08343997B2
Source datasetuspto-grants-2013_01
ORD IDord-f1c187a9cd5a4096b4646c7aaf1c658f
Source noteuspto-grants-2013_01