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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854557Generated: October 30, 2026

Tributylphosphine → 3-{4-[4-Ethyl-2-(4-trifluoromethyl-phenyl)-oxazol-5-ylmethoxy]-2-methyl-phenyl}-propionic acid methyl ester

https://huagongshe.com/reaction/854557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
ReactantMethyl 3-(4-Hydroxy-2-methylphenyl)propanoateHCID 13551833—
Reactant[4-Ethyl-2-(4-trifluoromethyl-phenyl)-oxazol-5-yl]-methanolHCID 58765785—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
Product3-{4-[4-Ethyl-2-(4-trifluoromethyl-phenyl)-oxazol-5-ylmethoxy]-2-methyl-phenyl}-propionic acid methyl esterHCID 58626636—

Reaction Steps

To a solution of [4-Ethyl-2-(4-trifluoromethyl-phenyl)-oxazol-5-yl]-methanol (0.108 g, 0.400 mmole) and 3-(4-Hydroxy-2-methyl-phenyl)-propionic acid methyl ester (0.078 g, 0.400 mmole) in toluene (2 mL) at room temperature, is added tributylphosphine followed by a solution of 1,1′-(azodicarbonyl)-dipiperidine (0.201 g, 0.8 mmole) in toluene (2 mL). The reaction is stirred overnight, then diluted with hexane (10 mL). The precipitate is removed through filtration and the filtrate is concentrated, loaded to a silica gel column, eluted with ethyl acetate in hexane (0-15%) and concentrated to provide the titled compound as a white solid. Mass [EI+] 448 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259175B2
Source datasetuspto-grants-2007_08
ORD IDord-10b65dbb66f045b3915046b58857ef1a
Source noteuspto-grants-2007_08