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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044762Generated: October 30, 2026

Nitrogen → 2-(2-Methyl-[1,3]dioxolan-2-yl)-oxazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1044762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantTrimethyl orthoformateHCID 9005—
ReactantSodium CarbonateHCID 10340—
ReactantEthyl 2-acetyloxazole-4-carboxylateHCID 66820192—
SolventEthylene GlycolHCID 174—
Product2-(2-Methyl-[1,3]dioxolan-2-yl)-oxazole-4-carboxylic acid ethyl esterHCID 66819900—

Reaction Conditions

Temperature95 °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-acetyl-oxazole-4-carboxylic acid ethyl ester (7.0 g, 38.0 mmol) in ethylene glycol (42.7 mL) was treated with trimethylorthoformate (10.5 mL, 96.0 mmol) followed by LiBF4 (0.73 g, 8.0 mmol). The reaction mixture was heated at 95° C. until completion of the reaction. Aq. 0.5 M Na2CO3 was added and the mixture was extracted with Et2O. The org. layer was washed with aq. 0.5 M Na2CO3 (2×), dried over Na2SO4, filtered, and the solvent was removed under reduced pressure to give the title compound as a yellow oil. LC-MS-conditions 01: tR=0.76 min; [M+H]+=227.99.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563714B2
Source datasetuspto-grants-2013_10
ORD IDord-aeb10fd890e44974be64d3c572474ce5
Source noteuspto-grants-2013_10