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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197661Generated: October 31, 2026

Triethylamine → methanesulfonic acid (R)-1-carbamoyl-propyl ester

https://huagongshe.com/reaction/2197661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(R)-2-HydroxybutanamideHCID 10898665—
SolventTetrahydrofuranHCID 8028—
Productmethanesulfonic acid (R)-1-carbamoyl-propyl esterHCID 86617530—

Reaction Conditions

Temperature20 °C

Reaction Steps

To a mixture of (R)-2-hydroxybutyramide (4.2 g, 40.7 mmol) and triethylamine (6.2 ml, 44.8 mmol, 1.1 equiv.) in tetrahydrofuran (50 ml) is added drop wise at −40° C. methanesulfonic acid chloride (3.5 ml, 44.8 mmol, 1.1 equiv.). The mixture is allowed to warm to 20° C. and is filtered over magnesium sulfate (8 g). The cake is rinsed twice with tetrahydrofuran (2×20 ml) and combined filtrates are concentrated to dryness under reduced pressure to afford methanesulfonic acid (R)-1-carbamoyl-propyl ester (IIi) as a solid. (7.9 g, 106%, triethylamine hydrochloride salts are present).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338621B2
Source datasetuspto-grants-2012_12
ORD IDord-05b4c13ae3744d27a8a2baa3117718fa
Source noteuspto-grants-2012_12