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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418790Generated: October 26, 2026

1-Bromopropane → N-benzyloxycarbonyl-3-[4-propoxyphenyl]-alanine-methyl ester

https://huagongshe.com/reaction/1418790

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromopropaneHCID 7840—
ReactantSodium hydrideHCID 24758—
ReactantSodium BicarbonateHCID 516892—
ReactantN-[(Phenylmethoxy)carbonyl]-L-tyrosine methyl esterHCID 7010613—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-benzyloxycarbonyl-3-[4-propoxyphenyl]-alanine-methyl esterHCID 22940772—

Reaction Steps

4.94 g (15 mmol) of N-benzyloxycarbonyl-tyrosine-methyl ester is dissolved in 25 ml of anhydrous N,N-dimethylformamide and mixed at 5° C. under argon with 0.61 g (15.5 mmol) of sodium hydride dispersion (60% in mineral oil). The batch is allowed to stir for 10 minutes, then 1.91 g (15.5 mmol) of propyl bromide is added, the reaction temperature is allowed to increase to room temperature and it is stirred for another two hours. For working-up, the batch is taken up in ethyl acetate and shaken out several times against aqueous sodium bicarbonate solution. The organic phase is separated, dried on magnesium sulfate, filtered and concentrated by evaporation. The residue is chromatographed for purification on silica gel with hexane/diethyl ether/triethylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05885548
Source datasetuspto-grants-1999_03
ORD IDord-1b1b6d4e4479430986678588eb86f835
Source noteuspto-grants-1999_03