HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 19776189, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 2-Naphthalenethiol | HCID 7058 | — |
| Reactant | Dibutylamine | HCID 8148 | — |
| Reactant | 2,6-Di-tert-butylphenol | HCID 31405 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19776189 | HCID 19776189 | — |
Reaction Steps
Thio-2-naphthol (16.0 g, 0.1 mol), 2,6-di-tertbutylphenol (20.6 g, 0.1 mol), paraformaldehyde (3.0 g, 0.1 mol) and di-n-butylamine (1 ml) in ethanol (100 ml) are heated, under reflux for thirteen hours, after which time thin layer chromatography shows the reaction to be complete. A small amount of solid impurity is filtered off and the solvent removed by rotary evaporation. A yellow oil is left which solidifies below 30° C. Petroleum (40°-60°) is added and a white solid (20.9 g, 55% of theory) of m.p. 30° C. is collected.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05190723 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-79a9dce58727458b8c914d029e8185a2 |
| Source note | uspto-grants-1993_03 |