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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450603Generated: November 3, 2026

Trifluoroacetic acid → HCID 9849492, compound

https://huagongshe.com/reaction/1450603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67708481HCID 67708481—
SolventDichloromethaneHCID 6344—
ProductHCID 9849492HCID 9849492—

Reaction Steps

A solution of 1.4 g (2.4 mMol) of tert.butyl 4'-[(2-ethyl-4-methyl-6-(1-methyl-5-fluoro-benzimidazol-2-yl)-benzimidazol-1-yl)-methyl]-biphenyl-2-carboxylate and 15 ml of trifluoroacetic acid in 30 ml of methylene chloride is stirred for 14 hours at ambient temperature, then concentrated by evaporation, the residue is mixed with about 30 ml of water and made alkaline with 2N sodium hydroxide solution. After extracting twice with 30 ml of diethyl ether, the aqueous phase is acidified with 20% citric acid. The crude product precipitated is suction filtered and purified by column chromatography (100 g silica gel; eluant:methylene chloride/ethanol=96:4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602127
Source datasetuspto-grants-1997_02
ORD IDord-2bd3b9e3e0204978b8b5841be0e235bf
Source noteuspto-grants-1997_02