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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283949Generated: October 29, 2026

p-Toluenesulfonic acid monohydrate → Benzyl 4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-(2-oxoethyl)-1H-imidazol-2-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2283949

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantBenzyl 4-(1-((1,3-dioxolan-2-yl)methyl)-4-(4-fluoro-3-(trifluoromethyl)phenyl)-1H-imidazol-2-yl)piperidine-1-carboxylateHCID 89442873—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductBenzyl 4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-(2-oxoethyl)-1H-imidazol-2-yl)piperidine-1-carboxylateHCID 89445521—

Reaction Conditions

Temperature50 °C

Reaction Steps

The reaction mixture of benzyl 4-(1-((1,3-dioxolan-2-yl)methyl)-4-(4-fluoro-3-(trifluoromethyl)phenyl)-1H-imidazol-2-yl)piperidine-1-carboxylate (1450.00 mg; 2.72 mmol; 1.00 eq.) and toluene-4-sulfonic acid monohydrate (5169.79 mg; 27.18 mmol; 10.00 eq.) in 30 ml of acetone and 2.5 ml of water was stirred at 50° C. for one week. LC-MS showed some a mixture of the desired product, ˜30% of starting material and some by products. The reaction mixture was concentrated and added 50 ml water, extracted with EA. The combined organic layers were washed with brine, dried and concentrated. The residue was subjected to SNAP column (100 g), eluted with 0-100% EA in hexane, then eluted with 10% methanol in DCM to afford the tile compound as yellow oil (480 mg, yield 36%) with a recovery of some starting material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145392B2
Source datasetuspto-grants-2015_09
ORD IDord-2eccf8a067e04e60bce653f87e8bb123
Source noteuspto-grants-2015_09