HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233304Generated: October 31, 2026
Trifluoroacetic acid → HCID 59295393, compound
https://huagongshe.com/reaction/2233304
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 2-Chloro-4-hydroxybenzonitrile | HCID 592797 | — |
| Reactant | HCID 59295386 | HCID 59295386 | — |
| Reactant | HCID 59295436 | HCID 59295436 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59295393 | HCID 59295393 | 100.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07709481B2 |
|---|
| Source dataset | uspto-grants-2010_05 |
|---|
| ORD ID | ord-1ea92bcff98f40d0b59cc1ded35fedf6 |
|---|
| Source note | uspto-grants-2010_05 |
|---|