Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613358Generated: October 30, 2026

Benzene → 3-Methyl-3-oxetanylmethyl 3-benzyloxypropionate

https://huagongshe.com/reaction/613358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant3-(Benzyloxy)propanoic acidHCID 15608813—
Product3-Methyl-3-oxetanylmethyl 3-benzyloxypropionateHCID 54178956—

Reaction Steps

Oxalyl chloride (880 mg) was added to a solution of 3-benzyloxypropionic acid (1.04 g) in benzen (10 ml). Subsequently, dimethylformamide (100 mg) was added. After the resultant mixture was stirred for 30 minutes at room temperature, benzen was distilled off. Azeotropic distillation was performed twice through use of benzen (10 ml), and the resultant residue was dissolved in tetrahydrofuran (10 ml). To the solution were added 3-methyl-3-oxetanyl-methyl alcohol (620 mg) and then triethylamine (620 mg). The mixture was stirred for 5 hours at room temperature. Ethyl acetate was added to the reaction mixture, followed by washing with sat. aq. K2CO3, water, 1N-HCl, water, and saturated brine and then drying over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate-hexane 2:1), to give 1.01 g of 3-methyl-3-oxetanylmethyl 3-benzyloxypropionate as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008224
Source datasetuspto-grants-1999_12
ORD IDord-1fd6926837e84342af55af17129fd240
Source noteuspto-grants-1999_12