Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254526Generated: November 2, 2026

Trifluoroacetic acid → N-Methyl-L-Alanyl-L-Alanine benzyl Ester

https://huagongshe.com/reaction/2254526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantBenzyl (S)-2-[(S)-2-(tert-butoxycarbonyl-methyl-amino)-propanoylamino]-propionateHCID 14673102—
SolventDichloromethaneHCID 6344—
ProductN-Methyl-L-Alanyl-L-Alanine benzyl EsterHCID 14673104—

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a stirred solution of 17 g (0.0466 mole) of Boc-N-methyl-L-alanyl-L-alanine benzyl ester in 150 ml of dry dichloromethane, cooled at -10° C., was added 100 ml trifluoroacetic acid, which was previously cooled at -10° C. The reaction mixture was stirred for 16 hours at -5° C., then poured carefully with good stirring into a mixture of 177 g of sodium bicarbonate, ice, and 150 ml of dichloromethane. The organic layer was separated and the aqueous layer was further extracted with another 60 ml of dichloromethane. The combined organic layers were washed with 3×50 ml of saturated sodium bicarbonate solution, dried over mangesium sulfate, and evaporated to give 11.6 g (91% of theory) of crude product which was used in step 3 without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05236899
Source datasetuspto-grants-1993_08
ORD IDord-9cd9226e46a0475ebf8ee0d0a4e851df
Source noteuspto-grants-1993_08