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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233304Generated: October 31, 2026

Trifluoroacetic acid → HCID 59295393, compound

https://huagongshe.com/reaction/2233304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-Chloro-4-hydroxybenzonitrileHCID 592797—
ReactantHCID 59295386HCID 59295386—
ReactantHCID 59295436HCID 59295436—
SolventDichloromethaneHCID 6344—
ProductHCID 59295393HCID 59295393100.2%

Reaction Steps

4.5 g 4-[5-(3-Chloro-4-cyano-phenoxymethyl)-4-methyl-thiazol-2-yl]-piperidine-1-carboxylic acid tert-butyl ester (derived from 4-(5-Chloromethyl-4-methyl-thiazol-2-yl)-piperidine-1-carboxylic acid tert-butyl ester and commercially available 2-Chloro-4-hydroxy-benzonitrile according to the method described in Example 1) was dissolved in 100 ml dichloromethane. 20 ml trifluoroacetic acid were added and the reaction mixture stirred at room temperature for one hour. The solvent was removed in vacuo and the residue was dissolved in 200 ml ethyl acetate, washed three times with saturated NaHCO3 solution and then dried over MgSO4. The solvent was removed in Vacuo to obtain 3.5 g 2-Chloro-4-(4-methyl-2-piperidin-4-yl-thiazol-5-ylmethoxy)-benzonitrile as colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709481B2
Source datasetuspto-grants-2010_05
ORD IDord-1ea92bcff98f40d0b59cc1ded35fedf6
Source noteuspto-grants-2010_05