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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044763Generated: November 1, 2026

Nitrogen → (2-(2-Methyl-[1,3]dioxolan-2-yl)oxazol-4-yl)methanol

https://huagongshe.com/reaction/1044763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant2-(2-Methyl-[1,3]dioxolan-2-yl)-oxazole-4-carboxylic acid ethyl esterHCID 66819900—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(2-(2-Methyl-[1,3]dioxolan-2-yl)oxazol-4-yl)methanolHCID 66820136—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), to an ice-cold solution of 2-(2-methyl-[1,3]dioxolan-2-yl)-oxazole-4-carboxylic acid ethyl ester (5.05 g, 22.2 mmol) in dry THF (80 mL) was added an ice-cold solution of LiAlH4 (1.0 M in THF, 24.7 mL, 24.7 mmol). The reaction mixture was stirred at 0° C. until completion of the reaction. Water (2.0 mL) was carefully added at 0° C. followed by aq. 1 M NaOH (2.0 mL) and water (2.0 mL). The resulting suspension was stirred at rt for 1 h, filtered (+EA) and the filtrate concentrated under reduced pressure to give the title compound as a yellow oil. TLC: rf (EA)=0.18. LC-MS-conditions 05c: tR=0.22 min; [M+H]+=186.30.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563714B2
Source datasetuspto-grants-2013_10
ORD IDord-44a6f4e341a94c2c802883bf2b2b098d
Source noteuspto-grants-2013_10