HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 499187Generated: October 30, 2026
Trifluoroacetic acid → HCID 23103401, compound
https://huagongshe.com/reaction/499187
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | {4-[1-(2,6-Dichloro-benzoyl)-piperidin-4-yloxy]-phenyl}-carbamic acid tert-butyl ester | HCID 59420870 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23103401 | HCID 23103401 | 92% |
Reaction Steps
The above white solid, {4-[1-(2,6-dichloro-benzoyl)-piperidin-4-yloxy]-phenyl}-carbamic acid tert-butyl ester, is suspended in a solution of trifluoroacetic acid in dichloromethane (25% v/v, 20 mL). The reaction mixture is stirred at 22° C. for 15 min. After removal of the solvent, the oily residue is neutralized with 0.5 N aqueous sodium hydroxide solution (50 mL) and extracted with dichloromethane (5×50 mL). The combined organic phases are dried over anhydrous sodium sulfate and concentrated to yield a yellow solid (440.2 mg, 92.0% yield, ES+(m/z) 365.1 [M+H]).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07767674B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-a8eb332209a84b3aa709d5b81503900b |
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| Source note | uspto-grants-2010_08 |
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