HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 54421573, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 2,4,4-Trimethyl-1-pentene | HCID 7868 | — |
| Reactant | p-Isopropenylphenol | HCID 584247 | — |
| Product | HCID 54421573 | HCID 54421573 | — |
Reaction Steps
134 g (0.5 mol) of molten dimeric 4-isopropenylphenol and 120 g (1.07 mol) of diisobutylene are simultaneously added dropwise over a period of 4 hours at around 90° C to a suspension of 20 g of an acid-activated fuller's earth in 100 ml of toluene. The mixture is then left to react for another 2 hours at 90° C, after which the catalyst is filtered off and the solvent distilled off. Fractional distillation of the residue gives a fraction which distills over at 160°-170° C./12 Torr and subsequently solidifies in crystalline form. Recrystallisation from petroleum ether gives 41.2 g (34 % of the theoretical) of 5-hydroxy-1,1,3-trimethyl-3-neopentyl indane (IV) melting at 102° C. ##STR22##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04045499 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-b1c7d67e89c144ee93ff6795bf206d10 |
| Source note | uspto-grants-1977_08 |