Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843338Generated: October 30, 2026

Trifluoroacetic acid → HCID 12992466, compound

https://huagongshe.com/reaction/843338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 18727512HCID 18727512—
SolventDichloromethaneHCID 6344—
ProductHCID 12992466HCID 1299246697.7%

Reaction Steps

N-tert-Butoxycarbonyl-N-methyl-2-aminoacetic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide (65) (2.19 g; 4.99 mmol) is dissolved in methylene chloride (30 mL) at ambient temperature. Trifluoroacetic acid (20 mL) is added in a slow stream, and the solution is stirred for 2.5 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 white solid. CIMS: MH+ 339

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376514B1
Source datasetuspto-grants-2002_04
ORD IDord-fe1c64fb61b64f0f8f3bf57229d4a32e
Source noteuspto-grants-2002_04