Tributylstannane → 4-Heptylbenzaldehyde

To a stirred solution of 6.60 g (30 mmol) of 4-heptylbenzoic acid (obtained from Aldrich Chemical Company (#23,064-2) and used without purification) in 50 mL of dichloromethane at room temperature under nitrogen was added 4.0 mL (45 mmol, 1.5 equivalents) of oxalyl chloride and then 0.1 mL (1.3 mmol) of DMF. The resulting vigorously bubbling solution was stirred for 1 h and then evaporated. The semi-solid residue was dissolved in 40 mL of benzene under argon and 350 mg (0.31 mmol) of tetrakis(triphenylphosphine)palladium was added. To this stirring solution at room temperature was added 11.1 mL (34 mmol) of tributyltin hydride over 20 min. The solution turns yellow and warms autogenously to 40° C. After 1 h, the reaction was treated with 100 mL of 10% aqueous potassium fluoride and stirred vigorously for 30 min. The reaction mass was filtered, the filtrate diluted with ether, washed with water, and the organic layer separated, dried (MgSO4) and evaporated onto 10 g of silica gel. Purification by flash chromatography (5×20 cm column, 3:7 dichloromethane/hexanes as elutent) gave 5.95 g, 97% yield, of title compound as a colorless oil.

1. customevaporated
2. dissolutionThe semi-solid residue was dissolved in 40 mL of benzene under argon
3. customautogenously to 40° C
4. waitAfter 1 h
5. stirringstirred vigorously for 30 min
6. filtrationThe reaction mass was filtered
7. additionthe filtrate diluted with ether
8. washwashed with water
9. customthe organic layer separated
10. dry with materialdried (MgSO4)
11. customevaporated onto 10 g of silica gel
12. customPurification by flash chromatography (5×20 cm column, 3:7 dichloromethane/hexanes as elutent)
13. customgave 5.95 g, 97% yield

ORD-Eintrag

ord-3461f820a2c04229a62965436792cfba

Quelldatensatz

uspto-grants-1996_10

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US05567841