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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903366Generated: October 25, 2026

Methanol → Methyl (2S)-2-amino-3-(4-fluorophenyl)propanoate

https://huagongshe.com/reaction/1903366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantThionyl ChlorideHCID 24386—
Reactant4-fluoro-L-phenylalanineHCID 716312—
ProductMethyl (2S)-2-amino-3-(4-fluorophenyl)propanoateHCID 7018988—

Reaction Conditions

Temperature-10 °C

Reaction Steps

1.8 g (10 mmole) of 4-fluorophenylalanine is suspended in 3.0 ml of methanol and cooled to -10° C. under nitrogen and 0.81 ml of thionylchloride added dropwise, keeping the temperature at or below -2° C., and stirred for 1 hour at -5° C to -10° C. About 10 ml of methanol was added and the solution stirred at room temperature overnight. The solution was concentrated in vacuo and the residue triturated with dry ether and filtered to give the hydrochloride salt of 4-fluorophenylalanine methyl ester, m.p. 177.5 to 178° C. The ester hydrochloride is substituted for L-phenylalanine methyl ester hydrochloride in the procedure of Example 6a to yield 6b.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04435571
Source datasetuspto-grants-1984_03
ORD IDord-1268c11a6ee5464fb98f48f1072a3221
Source noteuspto-grants-1984_03