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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648178Generated: October 30, 2026

Trifluoroacetic acid → O-methoxymethyl-N-methyl-beta-benzoyloxytyrosine methyl ester

https://huagongshe.com/reaction/1648178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantThiophenolHCID 7969—
ReactantSodium BicarbonateHCID 516892—
ReactantO-methoxymethyl-N-methyl-N-(2-nitrophenylthio)-beta-benzoyloxytyrosine methyl esterHCID 54000197—
SolventDichloromethaneHCID 6344—
ProductO-methoxymethyl-N-methyl-beta-benzoyloxytyrosine methyl esterHCID 538672819.1%

Reaction Steps

To a solution of O-methoxymethyl-N-methyl-N-(2-nitrophenylthio)-β-benzoyloxytyrosine methyl ester (threo isomer) (4.94 g) in dichloromethane (50 ml) were added thiophenol (4.8 ml) and trifluoroacetic acid (2.5 ml) at 0° C. After stirring for 30 minutes, sodium bicarbonate aqueous solution was added to the mixture. The organic layer was washed with sodium bicarbonate aqueous solution and brine. After evaporating, the residue was put on a column of silica gel (MERCK 7734, 100 g) and eluted with 5% methanol in chloroform to give O-methoxymethyl-N-methyl-β-benzoyloxytyrosine methyl ester (threo isomer) (0.32 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436140
Source datasetuspto-grants-1995_07
ORD IDord-c5d0c30df5ac46ec97f649a03af17fbe
Source noteuspto-grants-1995_07