HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → 1,1,3,3-Tetramethylindan-5-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Bisphenol A | HCID 6623 | — |
| Reactant | 4-tert-Butylphenol | HCID 7393 | — |
| Product | 1,1,3,3-Tetramethylindan-5-ol | HCID 104567 | 19.9% |
Reaction Steps
172.5 g of 4-tert.-butylphenol, 57.5 g of 2,2-bis-(4-hydroxyphenyl)-propane and 20 g of p-toluene sulphonic acid are stirred in an autoclave for 6 hours at around 180° C. After cooling, the reaction mixture is repeatedly washed with about 250 ml of 10 % by weight aqueous sodium hydrogen carbonate solution to remove the catalyst, and then subjected to fractional distillation in vacuo. 9.3 g (0.05 mol) of 5-hydroxy-1,1,3,3-tetramethyl indane are isolated from 157.7 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-860c3af05d6748d7bad68e212ccd9fd7 |
| Source note | uspto-grants-1977_08 |