HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222575Generated: October 28, 2026
Trifluoroacetic acid → HCID 66865450, compound
https://huagongshe.com/reaction/222575
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Piperidinecarboxylic acid, 4-[[4-[1,2,3,6-tetrahydro-1-(methylsulfonyl)-4-pyridinyl]phenoxy]methyl]-, 1,1-dimethylethyl ester | HCID 66864688 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66865450 | HCID 66865450 | 88.5% |
Reaction Steps
Trifluoroacetic acid (2.98 g, 1.97 mL, 26.10 mmol) is added to a solution of 4-[4-(1-methanesulfonyl-1,2,3,6-tetrahydro-pyridin-4-yl)-phenoxymethyl]-piperidine-1-carboxylic acid tert-butyl ester (1.20 g, 2.61 mmol) in dichloromethane (13 mL). The mixture is stirred at 23° C. for 30 min. 2 M aq. sodium hydroxide is added. The resulting white precipitate is filtered and washed with water. The mother liquor is extracted with dichloromethane. The combined organic layers are dried over anhydrous sodium sulfate, filtered, and the solvent is removed to obtain a white solid which is combined with the initial precipitate and dried under high vacuum for 16 h. Diethyl ether is added and the solid is filtered and washed with ethyl acetate to obtain 0.810 g of an off-white solid. MS (m/z) 351 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207344B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-5c024ea63cd54bffab2429acb24fa1ae |
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| Source note | uspto-grants-2012_06 |
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