HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → Diniconazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (E)-1-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-yl)-4,4-dimethyl-1-penten-3-one | HCID 11110117 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Diniconazole | HCID 6436605 | 80.7% |
Reaction Steps
To 50 cc of a methanol solution containing 3.2 g of (E)-1-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-yl)-4,4-dimethyl-1-penten-3-one (melting point 92°-93° C.) characterized by the NMR spectrum shown below, was added 0.5 g of sodium borohydride, while cooling in ice. The mixture was then stirred at room temperature for 3 hours and treated as in Reference Example 1 to obtain 2.6 g of the captioned compound melting at 148°-149° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04435203 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-8cb1a6da61f5431eaef1a8a467463c17 |
| Source note | uspto-grants-1984_03 |