HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → Cyclopropyl-(3-methoxyphenyl)-(3-pyridinyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-(3-Methoxybenzoyl)pyridine | HCID 10036137 | — |
| Product | Cyclopropyl-(3-methoxyphenyl)-(3-pyridinyl)methanol | HCID 15552043 | — |
Reaction Steps
To a solution of (3-methoxyphenyl)-(3-pyridinyl)methanone (500 mg) in THF (10 ml) was added 1.1M cyclopropylmagnesium bromide THF solution (2 ml) at 0° C. The reaction mixture was warmed to room temperature, and stirred for 30 minutes. Aqueous ammonium chloride and ethyl acetate were added to the reaction mixture, the organic layer was separated and washed with saturated aqueous sodium chloride, and dried with magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was filtered and washed with ethyl acetate-hexane (1:2) to give cyclopropyl-(3-methoxyphenyl)-(3-pyridinyl)methanol (470 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06503926B2 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-cc63e8ec1ea0433c872301910b1cc01e |
| Source note | uspto-grants-2003_01 |