HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acrylonitrile → HCID 13061753, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Sulfur | HCID 5362487 | — |
| Reactant | HCID 13590129 | HCID 13590129 | — |
| Reactant | HCID 53684414 | HCID 53684414 | — |
| Product | HCID 13061753 | HCID 13061753 | — |
Reaction Steps
915 g N-isopropyl-N-(3-methyl-1,3-butadienyl)-carbamic acid methyl ester are heated without a solvent to 120° C. and 345 g acrylonitrile added dropwise. After completion of the addition the mixture is stirred for 1 hour at 140°. The resulting 2-(N-isopropyl-N-carbomethoxyamino)-4-methyl-3-cyclohexene-nitrile is heated at 200° and treated over a period of 2 hours portionwise with 386 g powdered sulphur. The reaction mixture is then stirred for 2 hours at 205° C. The resulting mixture is distilled under high vacuum at 110°-120° (0,1 torr), recrystallisation of the residue from benzine fraction yields the title product m.p. 100°-101°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04395550 |
| Source dataset | uspto-grants-1983_07 |
| ORD ID | ord-59a0077eb1674edab6e2cb5e4a47a175 |
| Source note | uspto-grants-1983_07 |