HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156201Generated: October 30, 2026
N-Methylacetamide → N-alpha-methoxyethyl-N-methyl-acetamide
https://huagongshe.com/reaction/1156201
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylacetamide | HCID 6582 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Chloro-1-methoxyethane | HCID 137067 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | N-alpha-methoxyethyl-N-methyl-acetamide | HCID 21464473 | — |
Reaction Steps
First 20 g of triethylamine and then a mixture of 91 g of triethylamine (1.1 moles in total) and 36.5 g (0.5 mole) of N-methylacetamide are added dropwise, at 0° C., to a solution of 94.5 g (1 mole) of α-chloroethyl methyl ether in 200 ml of hexane. After 2 hours, 44 g (1.1 moles) of technical-grade sodium hydroxide flakes are added and 20 ml of 50% strength sodium hydroxide solution are added dropwise, whilst cooling with ice, and the mixture is stirred for a further half an hour. The hexane solution is decanted, the flask is rinsed with hexane and the reaction solution is concentrated, the triethylamine employed being completely recovered in the distillate. The residue is subjected to flash distillation in vacuo. This yields 61 g (93% of theory) of N-α-methoxyethyl-N-methyl-acetamide. Boiling point (23 mm Hg): 84° C. 1H-NMR (CDCl3): 1.2-1.4 ppm (dd); 2.1 ppm (d); 2.8 ppm (d); 3.2 ppm (d); 4.95-5.15 ppm (q); 5.6-5.9 ppm (q).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04334097 |
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| Source dataset | uspto-grants-1982_06 |
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| ORD ID | ord-0a7d1996f3924a708ee293d020f44955 |
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| Source note | uspto-grants-1982_06 |
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