HuagongsheHuagongshe Chemistry Print Report · For research reference only
Catechol → 3,6-di-tert-butyl-catechol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Catechol | HCID 289 | — |
| Reactant | Isobutylene | HCID 8255 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 3,6-di-tert-butyl-catechol | HCID 3712192 | — |
Reaction Steps
A mixture of freshly distilled TiCl4 (11 g, 58 mmol) and pyrocatechol (13.7 g, 0.124 mol) was refluxed in 80 mL of xylene during 20 hours. The resulting dark-brown solid was filtered, washed by xylene and dried under vacuum. Titanium catecholate (10.24 g, 66%) was isolated. This salt (2.3 g, 8.7 mmol), pyrocatechol (82.5 g, 0.749 mol), xylene (80 mL) and isobutylene (150 mL) were heated in autoclave during 1.5 hours at 140° C. The solvent was removed and the residue was distilled under vacuum (b.p. −140-145° C., ˜1 mm Hg; m.p. 96-96.5° C.). Yield: 157.4 g (95%). (Also see “Organic Chemistry of Free Radicals”, Moscow, Khimia, 1979, p. 134.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07247687B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-32f7b01476244453ab0d2f43e6288ff9 |
| Source note | uspto-grants-2007_07 |