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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065080Generated: October 26, 2026

Ethylene Glycol → [5-(2-Methyl-[1,3]dioxolan-2-yl)-oxazol-2-yl]-methanol

https://huagongshe.com/reaction/2065080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantNitrogenHCID 947—
ReactantTrimethyl orthoformateHCID 9005—
ReactantHCID 131730010HCID 131730010—
SolventSodium BicarbonateHCID 516892—
Product[5-(2-Methyl-[1,3]dioxolan-2-yl)-oxazol-2-yl]-methanolHCID 66928789—

Reaction Conditions

Temperature95 °C

Reaction Steps

In a flame dried round-bottomed flask equipped with a magnetic stir bar and a condenser under inert atmosphere (N2), a solution of 1-[2-(tert-butyl-dimethyl-silanyloxymethyl)-oxazol-5-yl]-ethanone (105 mg, 0.41 mmol) in ethylene glycol (0.46 mL, 8.22 mmol) was treated with trimethylorthoformate (0.09 mL, 0.82 mmol) followed by LiBF4 (8 mg, 0.08 mmol). The reaction mixture was heated at 95° C. until reaction completion. Sat. aq. NaHCO3 (10 mL) was added and the mixture was extracted with EA (2×10 mL). The combined org. extracts were washed with brine (20 mL), dried over MgSO4, filtered, and the solvent was removed under reduced pressure. Purification of the residue by FC (4:1 EA-Hept) gave the title compound as a yellow oil. TLC: rf (4:1 EA-Hept)=0.25. LC-MS-conditions 02: tR=0.56 min; [M+H]+=186.55.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288419B2
Source datasetuspto-grants-2012_10
ORD IDord-6c69a5b57d744e838184d350738f1147
Source noteuspto-grants-2012_10