HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51279Generated: October 26, 2026
Trifluoroacetic acid → HCID 22737849, compound
https://huagongshe.com/reaction/51279
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | N-Boc-(2,3-dimethoxyphenyl)-4-piperidinylmethanone | HCID 46780868 | — |
| Product | HCID 22737849 | HCID 22737849 | 68.2% |
Reaction Steps
4-(2,3-dimethoxybenzoyl)-1-piperidinecarboxylic acid, 1,1-dimethylethyl ester (7) (˜0.1128 mol) was cooled to 0° C., treated with trifluoroacetic acid (85 mL), and stirred at ambient temperature for 1 hour. Following concentration in vacuum, the material was dissolved in water (300 mL), washed with hexane (2×110 mL) and then treated with solid sodium hydroxide (18 g). The resulting aqueous solution was then extracted with methylene chloride (3×170 mL). The combined organic extracts were washed with brine (220 mL), dried (MgSO4) and concentrated in vacuum. The resulting residue was dissolved in ethanol (110 mL), cooled to 0° C., treated with anhydrous hydrogen chloride gas until acidic, diluted with ether (110 mL) and stirred for 1 hour. The resulting solid was collected by filtration, then washed with a mixture of ethanol and ether (1:1, 110 mL) to afford 4-(2,3-dimethoxybenzoyl)piperidine (16) hydrochloride salt as a white solid (19.18 g, 53%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06713627B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-0d2d340ad4994888aa36206e33dd2281 |
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| Source note | uspto-grants-2004_03 |
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