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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072759Generated: October 31, 2026

Trifluoroacetic acid → N-Methyl-L-Leucyl-L-Valyl-N-Methyl-L-Alanyl-L-Alanine Benzyl Ester

https://huagongshe.com/reaction/2072759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantBoc-N-Methyl-L-Leucyl-L-Valyl-N-Methyl-L-Alanyl-L-Alanine Benzyl EsterHCID 14673110—
SolventDichloromethaneHCID 6344—
ProductN-Methyl-L-Leucyl-L-Valyl-N-Methyl-L-Alanyl-L-Alanine Benzyl EsterHCID 14673112—

Reaction Conditions

Temperature-15 °C

Reaction Steps

A solution of 15.7 g (0.0266 mole) of Boc-N-methyl-L-leucyl-L-valyl-N-methyl-L-alanyl-L-alanine benzyl ester in 125 ml of dry dichloromethane was stirred and cooled to -10° C. while 70 ml trifluoroacetic acid, previously cooled at -15° C., was added. After 2 hours, the reaction was carefully added with good stirring to a mixture of 105 g of sodium bicarbonate, ice, and 200 ml of dichloromethane. The organic layer was separated and the aqueous layer was extracted with another 50 ml of dichloromethane. The combined organic layers were washed with 3×80 ml of saturated sodium bicarbonate solution, dried over magnesium fulfate, and evaporated leaving 11.85 g (91% of theory) of product. The FAB m.s. showed a molecular ion peak at 491.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04914188
Source datasetuspto-grants-1990_04
ORD IDord-d2756f6f1d614957804b5ed4c06a9769
Source noteuspto-grants-1990_04