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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254528Generated: October 31, 2026

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

https://huagongshe.com/reaction/2254528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantBoc-L-Valyl-N-Mehtyl-L-Alanyl-L-Alanine Benzyl EsterHCID 14673106—
SolventDichloromethaneHCID 6344—
ProductL-Valyl-N-Methyl-L-Alanyl-L-Alanine Benzyl EsterHCID 14673108—

Reaction Conditions

Temperature-15 °C

Reaction Steps

A stirred solution of 17 g (0.0367 mole) Boc-L-valyl-N-methyl-L-alanyl-L-alanine benzyl ester in 170 ml of dry dichloromethane was cooled at -10° C. as 85 ml of trifluoroacetic acid, previously cooled at -15° C., was added. After 16 hours at -5° C., the reaction was carefully poured with good stirring into a mixture of 93 g of sodium bicarbonate, ice, and 250 ml of dichloromethane. The organic layer was separated and the aqueous layer was extracted with another 75 ml of dichloromethane. The combined organic layers were washed with 3×75 ml of saturated sodium bicarbonate solution, dried over magnesium sulfate, and evaporated to give 12.8 g (96% of theory) of crude product which was used in step 5 without further purification. FAB m.s. showed a molecular ion peak at 364.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05236899
Source datasetuspto-grants-1993_08
ORD IDord-b21d5bef50904eb5b4b794507c6b6a37
Source noteuspto-grants-1993_08