HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bisphenol A → 1,1,3,3-Tetramethylindan-5-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bisphenol A | HCID 6623 | — |
| Reactant | Isobutylene | HCID 8255 | — |
| Reactant | Tetraaluminum;trisilicate | HCID 21981400 | — |
| Product | 1,1,3,3-Tetramethylindan-5-ol | HCID 104567 | — |
Reaction Steps
114 g (0.5 mol) of 2,2-bis-(4-hydroxyphenyl)-propane, 90 g (1.6 mol) of isobutylene and 25 g of an aluminum silicate are stirred in an autoclave for 6 hours at around 300° C. under the naturally prevailing pressure. The catalyst is then filtered of while still hot. 41.8 g (44% of the theoretical) of 5-hydroxy-1,1,3,3-tetramethyl indane are isolated by fractional distillation in vacuo from the 170.9 g of reaction mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04045499 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-da79cdd7916748b591c4d5013ca7e1ad |
| Source note | uspto-grants-1977_08 |