HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1-Dimethoxyethyl(dimethyl)amine → (E)-1-(dimethylamino)ethylidenethiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1-Dimethoxyethyl(dimethyl)amine | HCID 87835 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (E)-1-(dimethylamino)ethylidenethiourea | HCID 10654343 | 76.5% |
Reaction Steps
N,N-Dimethyl acetamide dimethyl acetal (75 g, 0.56 mole) was added to a suspension of thiourea (33.0 g, 0.43 mole) in methylene chloride. The mixture was heated under reflux for 4 h. The solvent was removed and the residue was crystallized from 5% MeOH and diethyl ether affording (1E)-N′-(aminocarbonothioyl)-N,N-dimethylethanimidamide (47.8 g, 76% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08513266B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-e1d6d386fe2f4cb59de7edebe43b520a |
| Source note | uspto-grants-2013_08 |