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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189388Generated: October 30, 2026

Nitrogen → 2-Methanesulfonyloxymethyl-oxazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1189388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantEthyl 2-(hydroxymethyl)oxazole-4-carboxylateHCID 10511369—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product2-Methanesulfonyloxymethyl-oxazole-4-carboxylic acid ethyl esterHCID 86664911—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of 2-hydroxymethyl-oxazole-4-carboxylic acid ethyl ester (345 mg, 2.02 mmol) in dry CH2Cl2 (10 mL) was treated at 0° C. with Et3N (0.40 mL, 2.87 mmol) followed by DMAP (25 mg, 0.20 mmol) and Ms-Cl (0.20 mL, 2.60 mmol). After stirring at 0° C. for 2 h, the reaction was quenched with water (5 mL). The org. layer was dried over Na2SO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (1:2→1:1 EA-Hept) gave the title compound as a yellow solid. TLC: rf (1:1 EA-Hept)=0.23. LC-MS-conditions 01: tR=0.73 min; [M+H]+=249.94.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674111B2
Source datasetuspto-grants-2014_03
ORD IDord-476800d96fe441bbbee46117422a12d4
Source noteuspto-grants-2014_03