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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzene | HCID 241 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-(Benzyloxy)propanoic acid | HCID 15608813 | — |
| Product | 3-Methyl-3-oxetanylmethyl 3-benzyloxypropionate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06008224 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-1fd6926837e84342af55af17129fd240 |
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| Source note | uspto-grants-1999_12 |
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