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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620387Generated: November 2, 2026

Water → methyl(S)-3-tert-butoxycarbonylamino-2-morpholin-4-ylpropanoate

https://huagongshe.com/reaction/1620387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBis(2-chloroethyl) etherHCID 8115—
ReactantMethyl 3-((tert-butoxycarbonyl)amino)-L-alaninateHCID 7021143—
SolventDiisopropylethylamineHCID 81531—
Productmethyl(S)-3-tert-butoxycarbonylamino-2-morpholin-4-ylpropanoateHCID 6705634624.3%

Reaction Conditions

Temperature127 °C

Reaction Steps

2.8 g (20 mmol) of 1-chloro-2-(2-chloroethoxy)ethane are added to a solution of 5 g (20 mmol) of commercial methyl(S)-2-amino-3-tert-butoxycarbonylaminopropanoate in 65 ml of diisopropylethylamine. The reaction mixture is stirred at 127° C. for 18 h. After the addition of water, the reaction medium is extracted with ethyl acetate. The organic phases are combined, dried over sodium sulfate, filtered and evaporated. The residue obtained is purified by chromatography on silica gel, elution being carried out with a 70/30 heptane/ethyl acetate mixture. 1.4 g (24%) of methyl(S)-3-tert-butoxycarbonylamino-2-morpholin-4-ylpropanoate are obtained in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772478B2
Source datasetuspto-grants-2014_07
ORD IDord-1fab35d85d4e444faac3bb95a0ba71ef
Source noteuspto-grants-2014_07