HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 15581948, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | N-Methylaniline | HCID 7515 | — |
| Reactant | α-(1-Methylethyl)-2-pyridineethanethioamide | HCID 15581943 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 15581948 | HCID 15581948 | — |
Reaction Steps
A solution of 1.94 g. (0.01 mole) of 3-methyl-2-(2-pyridyl)thiobutanamide in 40 ml. of methanol is treated with 1.6 g. (0.015 mole) of N-methylaniline and 1.22 ml. of 37 percent formalin solution. The reaction is kept at 25°C. for 12 hours, then refluxed for four hours. The solvents are evaporated in vacuo and the residue is triturated with ethyl acetate and cooled, then filtered. The filtrate is evaporated in vacuo and the resulting oil is triturated with cold ether to give 3-methyl-N-(N-methyl-N-phenylaminomethyl)-2-(2-pyridyl)thiobutanamide, which after recrystallization from ether melts at 95°-97°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03931162 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-e9ec5e08a1824aeb825fce3ba8549337 |
| Source note | uspto-grants-1976_01 |