HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → [(alpha-methyl-4-chlorobenzylidene amino)oxy]-N-methyl acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | [(alpha-Methyl-4-chlorobenzylidene amino)oxy] acetic acid methyl ester | HCID 54127586 | — |
| Product | [(alpha-methyl-4-chlorobenzylidene amino)oxy]-N-methyl acetamide | HCID 131711728 | — |
Reaction Steps
A mixture of 5.0 g of the [(α-methyl-4-chlorobenzylidene amino)oxy] acetic acid methyl ester obtained by the method described in example 3 and 40 ml of 35% aqueous methylamine solution was stirred for 2 hours. The precipitated solid substance was then dissolved by thrice extracting the mixture with an ether chloroform mixture. The extract was washed thrice with water, dried over anhydrous sodium sulfate and then concentrated by evaporation. Crystallisation of the residue from a benzene petroleum ether mixture yielded the above substance. Melting point 115° C.-116° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04196216 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-0ca6f0ca90fb4d489ba0e0d3bf96082c |
| Source note | uspto-grants-1980_04 |