HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646104Generated: November 1, 2026
Acetyl chloride → N-(2,2-Dimethoxyethyl)-N-2-propen-1-ylacetamide
https://huagongshe.com/reaction/1646104
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-(2,2-Dimethoxyethyl)prop-2-en-1-amine | HCID 13334742 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(2,2-Dimethoxyethyl)-N-2-propen-1-ylacetamide | HCID 45120254 | 80% |
Reaction Steps
N-allyl-N-dimethoxyethyl amine (30% aqueous, 48.3 grams, 0.10 mole) was added to a glass reaction vessel fitted with a mechanical agitator. The agitator was started and sodium hydroxide (4.44 grams, 0.11 mole) was dissolved in the aqueous amine. Toluene (50 grams) was added and the mixture cooled to 0° to 5° C. Acetyl chloride (8.24 grams, 0.105 mole) was added over 10 minutes while maintaining the temperature below 5° C. The reaction mixture was stirred for 30 minutes at 5° C., agitation was stopped, and the mixture allowed to phase separate. The aqueous layer was discarded. Toluene was removed from the organic layer by rotary evaporation and 14.8 grams (0.08 mole) of N-allyl-N-dimethoxyethyl acetamide was isolated as confirmed by NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05177263 |
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| Source dataset | uspto-grants-1993_01 |
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| ORD ID | ord-b3fdc222ce294d688cf8c9f09bac0102 |
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| Source note | uspto-grants-1993_01 |
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