HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl 4'-(benzyloxy)-2',6,6'-trimethylbiphenyl-3-carboxylate → Methyl 4'-hydroxy-2',6,6'-trimethylbiphenyl-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl 4'-(benzyloxy)-2',6,6'-trimethylbiphenyl-3-carboxylate | HCID 23157680 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl 4'-hydroxy-2',6,6'-trimethylbiphenyl-3-carboxylate | HCID 23157223 | 103.7% |
Reaction Steps
A mixture of methyl 4′-(benzyloxy)-2′,6,6′-trimethylbiphenyl-3-carboxylate (255 mg, 0.71 mmol), 10% palladium-carbon (50% water-containing product, 25.5 mg) and ethanol (3 mL) was stirred overnight under a hydrogen atmosphere at room temperature. The catalyst was filtered off, and the filtrate was concentrated under reduced pressure. The residue was again subjected to the above-mentioned conditions (10% palladium-carbon (50% water-containing product, 127 mg), stirring time 2 hr) to give the title compound (199 mg, yield 100%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07786165B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-bba42aecde9f4d768d067b27b66dbbdc |
| Source note | uspto-grants-2010_08 |