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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957446Generated: November 1, 2026

Methyl iodide → HCID 12486321, compound

https://huagongshe.com/reaction/1957446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTetrahydrofuranHCID 8028—
Reactant3-(Benzyloxy)-1,2-propanediolHCID 98072—
ReactantPotassium tert-butoxideHCID 23665647—
ProductHCID 12486321HCID 12486321—

Reaction Steps

A solution of 10.0 g (0.055 mol) of DL-α-O-benzylglycerol in a little THF was added to a suspension of 15.38 g (0.137 mol) of potassium tert-butoxide in 300 mL of THF. The mixture was stirred for 1 hr at RT and 18.72 (0.132 mol) of iodomethane was added. A white solid immediately separated. The reaction was stirred for 10 hr at RT, cooled, carefully diluted with sodium chloride solution and extracted with ether. The organic layer was washed with water, 5% HCl, water and saturated NaCl and dried. The solvent was removed and the residue was purified by flash chromatography to give 1-benzyloxy-2,3-dimethoxypropane, 9.16 g (79%), as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05783589
Source datasetuspto-grants-1998_07
ORD IDord-0b6645d3e8824463bde3fe44e5363f48
Source noteuspto-grants-1998_07