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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1102Generated: October 23, 2026

1-Tetradecanol → 1,2-Epoxy-2-methyl-3-tetradecyloxypropane

https://huagongshe.com/en/reaction/1102

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-TetradecanolHCID 8209—
Reactant3-Chloro-2-methyl-1-propeneHCID 11241—
ReactantSodium hydrideHCID 24758—
Reactantm-Chloroperbenzoic acidHCID 70297—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product1,2-Epoxy-2-methyl-3-tetradecyloxypropaneHCID 1969460879.5%

Reaction Conditions

Temperature60 °C

Reaction Steps

A 200-ml flask equipped with a stirrer was charged with 10 g (46.6 mmol) of tetradecanol, 50 ml of dimethylformamide, 2.86 g (71.5 mmol) of 60% NaH and 5.96 g (65.8 mmol) of methallyl chloride. The contents were stirred at 60° C. for 15 hours. After completion of the reaction, the reaction mixture was added with water and subjected to extraction with hexane, and the solvent was distilled off under reduced pressure. The resultant residue was charged into a 300-ml flask equipped with a stirrer, and 12.24 g (70.9 mmol) of m-chloroperbenzoic acid and 200 ml of dichloromethane were added thereto. The resultant mixture was stirred at room temperature for 19 hours. Solids formed were separated by filtration, and the resultant solution was concentrated under reduced pressure and then purified by column chromatography on silica gel, thereby obtaining 10.54 g (yield: 79.4%) of 1,2-epoxy-2-methyl-3-tetradecyloxypropane as an intermediate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723497
Source datasetuspto-grants-1998_03
ORD IDord-cb6871243aa046c0acd17a0fc444cdcb
Source noteuspto-grants-1998_03