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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306245Generated: November 2, 2026

Trifluoroacetic acid → HCID 131723468, compound

https://huagongshe.com/reaction/2306245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 11092070HCID 11092070—
SolventDichloromethaneHCID 6344—
ProductHCID 131723468HCID 131723468—

Reaction Conditions

Temperature0 °C

Reaction Steps

(S)-3-(tert-Butoxycarbonylamino)-1-[3′-(tert-butyldimethylsilyloxy) biphen-2-yl]-2-oxopyrrolidine, as described above in Step E, (888 mg, 1.84 mmol) was dissolved in CH2Cl2 (20 mL), cooled to 0° C., and trifluoroacetic acid (4 mL) was added. After 3 hours, the reaction mixture was poured into saturated aqueous NaHCO3 and extracted with CH2Cl2 (3×). The combined organic extracts were dried over Na2SO4, filtered and concentrated in vacuo, to yield the above-titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441017B1
Source datasetuspto-grants-2002_08
ORD IDord-1aa260fb4ded4b81ac41a608d871a381
Source noteuspto-grants-2002_08