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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27943Generated: October 30, 2026

Dicyclohexylcarbodiimide → 3-Benzylpyrrolylmethyl 2-(5-fluoro-2-benzothienyl)-3-methylbutanoate

https://huagongshe.com/reaction/27943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-(5-Fluoro-2-benzothienyl)-3-methylbutanoic acidHCID 53723241—
Reactant3-Benzyl-1-pyrrolylmethanolHCID 54343081—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product3-Benzylpyrrolylmethyl 2-(5-fluoro-2-benzothienyl)-3-methylbutanoateHCID 53753001—

Reaction Steps

To a stirred solution of 3-benzylpyrrolyl methanol (1.8 mmol), 2-(5-fluoro-2-benzothienyl)-3-methylbutanoic acid (2.0 mmol) and 4-dimethylaminopyridine (2.0 mmol) in 20 ml of methylene chloride and 2 ml of DMF is added N,N'-dicyclohexylcarbodiimide (2.0 mml). The reaction mixture is stirred, under nitrogen, for about two hours and then filtered and extracted with water. The aqueous phase is extracted with ether. The combined organic phases are washed with saturated aqueous NaHCO3, water and saturated aqueous NaCl, dried over CaSO4 and solvent evaporated to yield 3-benzylpyrrolylmethyl 2-(5-fluoro-2-benzothienyl)-3-methylbutanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04224330
Source datasetuspto-grants-1980_09
ORD IDord-b306f7b542d648819f0f1e38cfa67467
Source noteuspto-grants-1980_09