HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexene → 1-Chloromethyl-5-chloropyrimidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexene | HCID 8079 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 1-(4-Chlorophenylsulfenyl)methyl-5-chloropyrimidin-2-one | HCID 4295276 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Chloromethyl-5-chloropyrimidin-2-one | HCID 20161334 | — |
Reaction Steps
Sulphuryl chloride (3.0 mmol) in dry dichloromethane (10.0 ml) was added to 1-(4-chlorophenylsulphenyl) methyl-5-chloropyrimidin-2-one (see Example 2) (3.0 mmol) in dry dichlormethane 30.0 ml) at -30° C. for 3 mins. The mixture was stirred at -25° C. for 50 mins before cyclohexene (3.5 mmol) in dry dichloromethane (10 ml) was added. After stirring for 15 mins the mixture was filtered, evaporated and the residue washed three times with Pet. ether. Insoluble 1-chloromethyl-5-chloropyrimidin-2-one (0.45 g), 84% was used in Example 31 without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04705791 |
| Source dataset | uspto-grants-1987_11 |
| ORD ID | ord-d75c67c27b92457c97baa372c3f2dee8 |
| Source note | uspto-grants-1987_11 |