HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triadimefon → Triadimenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triadimefon | HCID 39385 | — |
| Reactant | Triethylammonium formate | HCID 11084032 | — |
| Product | Triadimenol | HCID 41368 | 63.6% |
Reaction Steps
28.45 g (0.1 mol) of 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-one and 43.25 g (0.1 mol) of formic acid/triethylamine (5:2 addition compound) were heated to 145° to 150° C. for 4.5 to 5 hours. The reaction mixture was allowed to cool and was concentrated in vacuo. The residue was taken up in dilute sodium hydroxide solution and the mixture was extracted with methylene chloride. The organic phase was washed with water, dried over sodium sulphate and concentrated in vacuo. The residue was suspended in hot cyclohexane, the suspension was filtered hot and the solid was dried. 18.2 g (63.6% of theory) of 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-butan-2-ol of melting point 114°-116° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04371700 |
| Source dataset | uspto-grants-1983_02 |
| ORD ID | ord-85245272f8394fb79a7fafd46c69355d |
| Source note | uspto-grants-1983_02 |