HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 178441105, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2,6-Di-tert-butylphenol | HCID 31405 | — |
| Reactant | HCID 178528002 | HCID 178528002 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178441105 | HCID 178441105 | — |
Reaction Steps
5-Mercapto-3-phenyl-1,3,4-thiadiazole-2(3H) thione potassium salt (26.4 g, 0.1 mol), 2,6-di-tertbutylphenol (20.6 g, 0.1 mol), formalin (11 ml) and concentrated sulphuric acid (10 ml) in ethanol (100 ml) are heated, under reflux, for six hours. After this time, the ethanol is removed by rotary evaporation, and partitioned between ethyl acetate and water. The organic phase is dried over magnesium sulphate, filtered and the solvent removed in vacuo. A yellow oil is left (29.5 g, 66% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05190723 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-37d0f6bdfffd46e1a9f5dc2a2cb8a15d |
| Source note | uspto-grants-1993_03 |