HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720905Generated: November 1, 2026
Trifluoroacetic acid → HCID 18727496, compound
https://huagongshe.com/reaction/720905
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 18727508 | HCID 18727508 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18727496 | HCID 18727496 | 138% |
Reaction Steps
N-(N-tert-Butoxycarbonyl-piperidine-4-carbonyl)-(N-methyl)-2-aminoacetic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide (67) (1.46 g; 2.66 mmol) is dissolved in methylene chloride (30 mL) at ambient temperature. Trifluoroacetic acid (15 mL) is added in a slow stream, and the solution is stirred for 2 hours at ambient temperature. The solution is concentrated in vacuo at 40° C. The residue is dissolved in methylene chloride (200 mL) and poured onto saturated sodium bicarbonate solution. The pH is adjusted to 9 with saturated potassium carbonate solution. The mixture is shaken the layers separated. The water layer is extracted with methylene chloride (3×50 mL). The combined organic extracts are washed with water, dried over MgSO4, filtered, and concentrated in vacuo affording the desired product (1.65 g) as a clear oil. ESMS:MH+ 450.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07135483B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-fd412bb32ebd4ed79b93cbf4284fb9ab |
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| Source note | uspto-grants-2006_11 |
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