HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2167436Generated: October 31, 2026
Acetaldehyde → methyl 2-chloro-3-(2-methyl-2H-1,3,4-dioxazol-5-yl)-4-methylsulfonylbenzoate
https://huagongshe.com/reaction/2167436
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Reactant | Methyl 2-chloro-3-hydroxyiminomethyl-4-methylsulfonylbenzoate | HCID 86584467 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | methyl 2-chloro-3-(2-methyl-2H-1,3,4-dioxazol-5-yl)-4-methylsulfonylbenzoate | HCID 21111958 | — |
Reaction Steps
8.0 g (27.4 mmol) of methyl 2-chloro-3-(hydroxyiminomethyl)-4-methylsulfonylbenzoate in 150 ml of methylene chloride were admixed dropwise with 16.0 g (27.4 mmol) of a 12.5% strength sodium hypochlorite solution, and a spatula-tip of sodium acetate was added. After 1 hour, 34.4 g (0.74 mol) of acetaldehyde were added a little at a time within a period of 36 hours, and the mixture was slowly heated to 55° C. The mixture was subsequently stirred at room temperature for 48 hours, washed with water, dried and concentrated. The residue was then taken up in methylene chloride, 10.0 g (0.23 mol) of acetaldehyde and a spatula-tip of sodium acetate were added and the mixture was heated under reflux for 8 hours. After 72 hours, a further 10.0 g 5 (0.23 mol) of acetaldehyde were added and the mixture was stirred at room temperature. The mixture was subsequently washed with water, dried and concentrated. The residue was passed through silica gel (eluent: isopropanol:cyclohexane=1:9). This gave 5.0 g (55% of theory) of methyl 2-chloro-3-(2-methyl-2H-1,3,4-dioxazol-5-yl)-4-methylsulfonylbenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045465B1 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-ae8be4f4154a431ca1909461519bafd8 |
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| Source note | uspto-grants-2015_06 |
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