HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-6-methoxynaphthalene → (2-Fluoro-4-methoxyphenyl)(6-methoxy-2-naphthyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-6-methoxynaphthalene | HCID 78786 | — |
| Reactant | 2-Fluoro-4-methoxybenzaldehyde | HCID 2734873 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-Fluoro-4-methoxyphenyl)(6-methoxy-2-naphthyl)methanol | HCID 22285701 | 1,953% |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
n-Butyllithium (2.5 M, 16.9 mL) was added dropwise into a cold (−78° C.) solution of 2-bromo-6-methoxynaphthalene (10.0 g, 42.2 mmol), and THF (200 mL). The reaction mixture was stirred at −78° C. for 2 h, and then 2-fluoro-4-methoxybenzaldehyde (6.5 g, 42 2 mmol) in THF (10 mL) was added. The mixture was allowed to warm up to 0° C. stirred for 10 min, and then quenched with aqueous ammonium cholride. The mixture was poured into water, acidified with HCl (2N) and extracted with EtOAc. The organic extracts were dried over MgSO4. Evaporation and purification by flash chromatography (hexanes/EtOAc 3/1) gave a brown solid (12.2 g, 93% yield, m.p. 68-69° C.); MS m/e 312 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06960607B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-0176a36bd1764994a0db7dd75f3aa34d |
| Source note | uspto-grants-2005_11 |