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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 74117Generated: October 27, 2026

Dimethyl Sulfate → (R)-N-benzyl-2-(ethoxycarbonylamino)-3-methoxypropionamide

https://huagongshe.com/reaction/74117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium HydroxideHCID 14797—
Reactant(R)-N-benzyl-2-(ethoxycarbonylamino)-3-hydroxypropionamideHCID 53344986—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
Product(R)-N-benzyl-2-(ethoxycarbonylamino)-3-methoxypropionamideHCID 5334498770.96%

Reaction Steps

To a 500 mL three-neck round bottom flask, 7.2 g (0.027 mol) (R)-N-benzyl-2-(ethoxycarbonylamino)-3-hydroxypropionamide, 300 mL ethyl acetate, 27.2 g (0.216 mol) dimethyl sulfate, and 2.0 g tetrabutylammonium bromide were added in sequence. At a normal temperature, 24.8 g 50% potassium hydroxide (0.2214 mol) solution was added. After the reaction was completed, 100 mL water was added, and the mixture was stirred for several minutes, and stood for layering. An organic layer was separated, and washed with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The solvent was evaporated, to obtain a transparent oily substance, which was triturated with n-hexane, suction-filtered, washed, and dried, to obtain a white solid of 5.37 g (0.01916 mol). The molar yield was 70.96%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829226B2
Source datasetuspto-grants-2014_09
ORD IDord-97cd46039495446584bca2082a5cf2de
Source noteuspto-grants-2014_09