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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362229Generated: October 30, 2026

Trifluoroacetic acid → HCID 22868979, compound

https://huagongshe.com/reaction/362229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
ReactantHCID 22868973HCID 22868973—
ProductHCID 22868979HCID 22868979114%

Reaction Conditions

Temperature0 °C

Reaction Steps

Cold trifluoroacetic acid (TFA, 4 mL) and 0.36 mL of anisole (3.28 mmol) were added to 1.215 g (2.98 mmol) of N-methyl-N-benzyl-2-(S)-t-butyloxycarbonylamino-3-(3-indolyl)propionamide and the resulting solution was stirred at 0° C. for 15 min. The ice bath was removed and the solution was allowed to warm to room temperature. After 30 min the reaction mixture was concentrated and the residue was partitioned between saturated NaHCO3 and CH2Cl2. The organic layer was washed with brine, dried and concentrated leaving 1.044 g of the title compound which was used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05869489
Source datasetuspto-grants-1999_02
ORD IDord-c7c0e6045f034cd38c2a3de589d7939a
Source noteuspto-grants-1999_02