HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-(4'-Butoxybenzylidene)-bornan-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Camphor | HCID 2537 | — |
| Reactant | 4-Butoxybenzaldehyde | HCID 79813 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-(4'-Butoxybenzylidene)-bornan-2-one | HCID 54023586 | — |
Reaction Steps
A solution of 100 millimols (15.2 g) of camphor in 250 ml of toluene is heated for 1 hour at the boil with 100 mmols (5.4 g) of sodium methylate. After cooling, 100 mmols (17.8 g) of p-butoxybenzaldehyde are introduced and the mixture is heated at the reflux temperature for 4 hours. The reaction mixture is cooled and 50 ml of water are then added; the toluene phase is separated off, washed with water, dried over sodium sulphate and concentrated to dryness. The solid residue is crystallised from aqueous isopropanol. After drying, 12 g of a white powder, which melts at 62°, are collected.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04290974 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-382c3a0e1c58473397c3af31952ef314 |
| Source note | uspto-grants-1981_09 |