HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-Methyl-4-(2-methyl-benzyloxy)-benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Bromo-2-methyl-1-((2-methylbenzyl)oxy)benzene | HCID 59132749 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methyl-4-(2-methyl-benzyloxy)-benzaldehyde | HCID 86602460 | 22% |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
A 2.5M solution of n-BuLi (2.1 mL, 5.26 mmol) in THF was added dropwise to a −78° C. solution of 31.2 (1.46 g, 5.01 mmol) in THF (25 mL). The reaction was stirred at −78° C. for 15 minutes and then DMF (3.3 mL) was added. Cooling was removed after 5 minutes and the reaction was allowed to warm to room temperature. The reaction was partitioned between ethyl acetate and water and the aqueous layer was extracted 1 additional time with ethyl acetate. The combined organic layers were dried (Na2SO4) and concentrated. The resulting residue was purified via radial chromatography (5% ethyl acetate in hexanes0 to yield 269 mg (22%) of 2-Methyl-4-(2-methyl-benzyloxy)-benzaldehyde (31.3). LC/MSD m/e: 241.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07649110B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-ef8007be0cec414d9ce3e6d975620cdf |
| Source note | uspto-grants-2010_01 |