HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244112Generated: November 2, 2026
Sodium Hydroxide → 2-(benzo[d][1,3]dioxol-5-yl)-N-methoxy-N-methylacetamide
https://huagongshe.com/reaction/2244112
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Benzo-1,3-dioxole-5-acetic acid | HCID 76115 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | Benzo(1,3)dioxol-5-yl-acetyl chloride | HCID 2756584 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(benzo[d][1,3]dioxol-5-yl)-N-methoxy-N-methylacetamide | HCID 14918161 | 95.2% |
Reaction Steps
Thionyl chloride (39.6 g) and a drop of dimethylformamide were added to a solution of benzo(1,3)dioxol-5-yl-acetic acid (30.0 g) in toluene (200 ml) and then the mixture was stirred for 2.5 hours at 60° C., after distilling out the solvent, to yield unpurified benzo(1,3)dioxol-5-yl-acetyl chloride. A solution of sodium hydroxide (20.0 g) in water (150 ml) was added to a solution of N,O-dimethylhydroxylamine hydrochloride (19.5 g) in toluene (200 ml) at 0° C., and further the unpurified benzo(1,3)dioxol-5-yl-acetyl chloride was added thereto, and then the mixture was stirred for 3 hours. The reaction mixture was extracted with toluene and dried over anhydrous magnesium sulfate, and from which the solvent was evaporated to yield unpurified 2-benzo(1,3)dioxol-5-yl-N-methoxy-N-methylacetoamide (35.4 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07678810B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-7c2591c86c8e4bcf9c12c9c670fca1e6 |
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| Source note | uspto-grants-2010_03 |
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