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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849014Generated: October 25, 2026

Trifluoroacetic acid → HCID 178472615, compound

https://huagongshe.com/reaction/849014

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantEthyl (2-oxo-2-((2-oxopropyl)amino)acetyl)glycinateHCID 10823329—
SolventAcetic AcidHCID 176—
ProductHCID 178472615HCID 178472615—

Reaction Steps

A solution of 3.43 g (14.9 mmol) of 7-2, 1.15 mL (14.9 mmol) of TFA and 2.104 mL (14.9 mmol) of trifluoroacetic anhydride in 60 mL of acetic acid was heated to 80° C. under a slow stream of Ar for 7 h. After HPLC analysis of the reaction progress, an additional 766 μL (9.9 mmol) of TFA and 1.4 mL (9.9 mmol) of trifluoroacetic anhydride were added and the reaction mixture was heated for an additional 24 h. After standing at rt for several hours, the solvents were removed at reduced pressure, and the residue digested in 7 mL of acetic acid at 60° C. for 10 min, then 35 mL of isopropyl acetate (iPAc) was added dropwise to the warm mixture. After the addition, the slurry was allowed to cool to rt, filtered, and washed with 1:5 HOAc-iPAc. The solid was air dried to give 7-3 as an almost colorless solid: 1H NMR (CDCl3) δ 10.92 (br s, 1H), 6.185 (s, 1H), 4.66 (s, 2H), 4.25 (q, 2H, 7.1 Hz), 2.08 (s, 3H), 1.30 (t, 3H, 7.1 H

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06011038
Source datasetuspto-grants-2000_01
ORD IDord-58fe76e193cd487c8df26eb53d2faf72
Source noteuspto-grants-2000_01