Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 13728693 | HCID 13728693 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13728694 | HCID 13728694 | — |
Reaction Steps
To a cold (-70°) solution of 2-bromo-6-(1-(4-chlorophenyl)-3-dimethylaminopropyl)pyridine (1.44 g) under nitrogen in dry tetrahydrofuran (50 mL) was added with stirring a solution of n-butyllithium (2.4 mL, 1.7M in hexane). After an additional 5 min at -70°, dry dimethylformamide (1.5 mL) was added dropwise during 2 min. The solution was allowed to warm and then quenched with water (5 mL). The solvents were removed under reduced pressure and the residue was dissolved in methylene chloride (50 mL). This solution was extracted with water (3×25 mL), dried (Na2SO4), and concentrated to give crude 6-(1-(4-chlorophenyl)-3-dimethylaminopropyl)2-pyridine carboxaldehyde (formyl proton δ 10.05, 60 MHz, CDCl3) which was chromatographed on reverse phase (C18, Waters Prep 500, 60:40/acetonitrile:water, K1 =6.3 (C18 ; 70:30/acetonitrile:water).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04621094 |
|---|
| Source dataset | uspto-grants-1986_11 |
|---|
| ORD ID | ord-529e5457cccc4935b228000921644311 |
|---|
| Source note | uspto-grants-1986_11 |
|---|