HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Benzyloxy-4-t-butyl-2-(1-octenyl)benzofuran → 4-Tert-butyl-5-hydroxy-2-octylbenzofuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Benzyloxy-4-t-butyl-2-(1-octenyl)benzofuran | HCID 54308722 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Tert-butyl-5-hydroxy-2-octylbenzofuran | HCID 23442864 | 69% |
Reaction Steps
10% Palladium on carbon (1.1 g) was added to a solution of 5-benzoxy-4-tert-butyl-2-(1-octenyl)benzofuran (1.1 g, 2.9 mmol) in acetic acid (50 ml), and the mixture was stirred for 36 h under a hydrogen atmosphere. After filtering off the Pd on carbon, the solvent was distilled off with an evaporator. The concentrate was purified by silica gel chromatography (chloroform) to afford 4-tert-butyl-5-hydroxy-2-octylbenzofuran [600 mg (yield, 69%)] as a pale yellow oil. Mass 302(M+), 287, 57
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05574178 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-654044c7f52a410ca77eb26a111baa4e |
| Source note | uspto-grants-1996_11 |