HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofurfuryl alcohol → Methyl 4'-methyl-5-((tetrahydrofuran-2-yl)methoxy)biphenyl-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofurfuryl alcohol | HCID 7360 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Diisopropyl diazene-1,2-dicarboxylate | HCID 75555 | — |
| Reactant | Methyl 5-hydroxy-4'-methyl-[1,1'-biphenyl]-3-carboxylate | HCID 58187967 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 4'-methyl-5-((tetrahydrofuran-2-yl)methoxy)biphenyl-3-carboxylate | HCID 58187973 | — |
Reaction Steps
To a stirred solution of methyl 5-hydroxy-4′-methylbiphenyl-3-carboxylate (150 mg, 0.59 mmol), triphenylphosphine (150 mg, 0.59 mmol), tetrahydro-2-furanmethanol (60 mg, 0.59 mmol) in CH2Cl2 (8 mL) at rt was slowly added a solution of diisopropyl azodicarboxylate (200 mg, 1.0 mmol) in CH2Cl2 (3 mL). The mixture was stirred at room temperature overnight, and then concentrated in vacuo. The residue was purified by flash chromatography to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08946439B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-09489a175fb842d98f020a1074b6f0d9 |
| Source note | uspto-grants-2015_02 |