Tributyltin Chloride → 5-(4-Methyl-2,6,7-trioxabicyclo[2,2,2]oct-1-yl)-2-[tri(n-butyl)stannyl]furan

2-(4-Methyl-2,6,7-trioxabicyclo[2,2,2]oct-1-yl)furan (2.0 g, 10.2 mmol) was dissolved in THF (20 ml) and the solution was cooled to −78° C. n-Buli (1.6M solution in hexanes, 7.7 ml, 12.32 mmol) was added and the mixture stirred at −78° C. for 30 min, allowed to warm to 0° C. for 20 min. and then recooled to −78° C. The tributyltin chloride (3.5 ml, 4.68 g, 14.4 mmol) was added and stirring was continued at −78° C. for 15 min. The mixture was allowed to warm gradually to room temperature and stirring continued for three days. The reaction was quenched by the addition of water, and extracted with ethyl acetate. This solution was washed with water, dried (MgSO4), and concentrated in vacuo to give the title compound as a yellow oil (4.7 g, 9.7 mmol, 95%); δH [2H6]DMSO 6.52 (1H,d), 6.38 (1H,d), 3.96 (6H,s), 0.77-1.63 (30H,m).

1. additionwas added
2. temperatureto warm to 0° C. for 20 min.
3. customrecooled to −78° C
4. stirringstirring
5. waitwas continued at −78° C. for 15 min
6. temperatureto warm gradually to room temperature
7. stirringstirring
8. waitcontinued for three days
9. customThe reaction was quenched by the addition of water
10. extractionextracted with ethyl acetate
11. washThis solution was washed with water
12. dry with materialdried (MgSO4)
13. concentrationconcentrated in vacuo

ORD-Eintrag

ord-fa73696acc7e4bb580ecbae151507658

Quelldatensatz

uspto-grants-2001_01

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US06174889B1