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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943585Generated: November 1, 2026

Water → ethyl (2S)-2-{[(tert-butoxy)carbonyl]amino}-3-hydroxypropanoate

https://huagongshe.com/reaction/1943585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
ReactantN-[tert-butoxycarbonyl]-L-serineHCID 98766—
SolventDimethylformamideHCID 6228—
Productethyl (2S)-2-{[(tert-butoxy)carbonyl]amino}-3-hydroxypropanoateHCID 13819295—

Reaction Steps

To a solution of Boc-Ser-OH (0.3 g, 1.46 mmol, 1 eq) in dry DMF (4 ml) at 0° C., dry K2CO3 (0.22 g, 1.6 mmol, 1.1 eq) was added. The resulting white suspension was stirred for 15 minute and ethyl iodide (0.68 g, 0.35 ml, 4.38 mmol, 3 eq) was dropwise added. The cooling was removed and reaction mixture was stirred at room temperature under N2 for 24 h. To the formed white emulsion H2O was added, and the mixture extracted by EtOAc. The combined organic layer was washed by H2O and then brine, and dried over MgSO4. The solvent was evaporated and the obtained oil was dried overnight in high vacuum. Yield of the pure F—0.27 g (79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394790B2
Source datasetuspto-grants-2013_03
ORD IDord-2a522377b0ac4b24a36933462877dedf
Source noteuspto-grants-2013_03