HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 2-Thiocyanomethyl-3-allyl-4(3H)-quinazolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Thiocyanic acid, chloromethyl ester | HCID 76755 | — |
| Reactant | HCID 178456612 | HCID 178456612 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 2-Thiocyanomethyl-3-allyl-4(3H)-quinazolinone | HCID 20239510 | — |
Reaction Steps
To a mixture of 5.8 g (0.03 mole) 2-mercapto-3-allyl-4(3H)-quinazolinone (the product of Example 5) in 200 ml dimethoxyethane, 5.4 g (0.05 mole) chloromethyl thiocyanate and 2.4 g (0.05 mole) 50% sodium hydride were added. The resulting mixture was stirred overnight at ambient temperature, refluxed at 50° C. for 8 hours, stirred overnight, refluxed at 50° C. for 8 hours and stirred overnight. The reaction mixture was washed with water, extracted with methylene chloride, dried over magnesium sulfate and stripped. The oily residue was triturated with ether, to give the above-identified product, as a solid, melting point 73°-76° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04605657 |
| Source dataset | uspto-grants-1986_08 |
| ORD ID | ord-1d22afbe27e840f2a92de4ae2e8d78ce |
| Source note | uspto-grants-1986_08 |