HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 1-(6-Chloro-3-pyridylmethyl)-2-(1-nitro-2-trimethylsilylmethylthioethylidene)imidazolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Methanethiol, trimethylsilyl- | HCID 140342 | — |
| Reactant | 2-Chloro-5-{[2-(nitromethylidene)imidazolidin-1-yl]methyl}pyridine | HCID 180957 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(6-Chloro-3-pyridylmethyl)-2-(1-nitro-2-trimethylsilylmethylthioethylidene)imidazolidine | HCID 86747328 | 39.5% |
Reaction Steps
0.5 g of 1-(6-chloro-3-pyridylmethyl)-2-nitromethyleneimidazolidine, 0.18 g of 37% formaldehyde aqueous solution and 0.24 g of mercaptomethyl trimethylsilane were added to 15 ml of ethanol, and were reacted under reflux for 1 hour. After completing the reaction, the reaction liquor was cooled by ice to precipitate a crystal. The crystal thus precipitated was taken out by filtration, and was washed with a cold ethanol to obtain 0.3 g of the aimed product (Compound No. 20) having a melting point of from 162.3° to 164.3° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05256674 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-2ec39e5ff78f479f9ecbdbee58eab737 |
| Source note | uspto-grants-1993_10 |