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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065029Generated: October 31, 2026

Ethylene Glycol → HCID 131730003, compound

https://huagongshe.com/reaction/2065029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantNitrogenHCID 947—
ReactantTrimethyl orthoformateHCID 9005—
ReactantHCID 131729997HCID 131729997—
SolventSodium BicarbonateHCID 516892—
ProductHCID 131730003HCID 131730003—

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-[4-(tert-butyl-dimethyl-silanyloxymethyl)-pyridin-2-yl]-ethanone (1.78 g, 6.71 mmol) in ethylene glycol (7.14 mL, 127.95 mmol) was treated with trimethylorthoformate (1.50 mL, 13.67 mmol) followed by LiBF4 (128 mg, 1.34 mmol). The reaction mixture was heated at 95° C. overnight. Sat. aq. NaHCO3 (50 mL) was added and the mixture was extracted with EA (50 mL). The org. extracts were washed with brine (2×50 mL), dried over MgSO4, filtered, and the solvent was removed under reduced pressure. Purification of the residue by FC (20:1 to 1:1 hept-EA) gave the title compound as a yellow oil. TLC: rf (1:1 hept-EA)=0.50. LC-MS-conditions 02: tR=0.91 min, [M+H]+=310.40.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288419B2
Source datasetuspto-grants-2012_10
ORD IDord-4105e1f8c5b34a58a4781971126b105e
Source noteuspto-grants-2012_10