HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847161Generated: October 30, 2026
Pyridine → N,1-Dimethoxy-N-methylcyclopropane-1-carboxamide
https://huagongshe.com/reaction/847161
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | 1-Methoxycyclopropane-1-carbonyl chloride | HCID 19882458 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N,1-Dimethoxy-N-methylcyclopropane-1-carboxamide | HCID 19882457 | 85% |
Reaction Steps
10 g (74 mmol) of 1-methoxy-cyclopropane-carbonyl chloride are added at 20° C. with stirring to a mixture of 8 g (82 mmol) of N,O-dimethyl-hydroxylamine hydrochloride and 100 ml of absolute dichloromethane. 13 g (164 mmol) of absolute pyridine are then added dropwise at 0° C. The mixture is initially subsequently stirred at 20° C. for one hour and then at 40° C. for one hour, the precipitate is then filtered off and 100 ml of dichloromethane are added. The reaction mixture is washed with water, dried over sodium sulphate and concentrated by stripping off the solvent under reduced pressure. The remaining residue is subjected to a vacuum distillation. 10 g (85% of theory) of N-methoxy-N-methyl-1-methoxy-cyclopropanecarboxamide are obtained in this manner in the form of an oil having a boiling point of b.p.=125° C. at 20 mbar. ##STR35##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05140035 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-11a611742f544eeaa7e52bb448f7c4f9 |
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| Source note | uspto-grants-1992_08 |
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