Isopentyltriphenylphosphonium bromide → 9-Bromo-2-methyl-4-decene

Temperatur

-70 °C

n-Butyl lithium (1.5M solution in hexane, 6.8 ml) was added to a stirred suspension of (3-methylbutyl)-triphenylphosphonium bromide (4.1 g) in dry tetrahydrofuran (50 ml) at -60° C. under nitrogen. The dark mixture was stirred for 40 minutes at -70° C. then a solution of 6-bromohexanal (1.8 g) in dry tetrahydrofuran (6 ml) was added. The pale mixture was stirred for a further 1 hour at -70° C. then evaporated under vacuum. The residue was extracted with ether and the extract was evaporated to a pale oil which was chromatographed on silica gel, eluting with 1:1 ether:hexane, to give the title compound as a colourless oil. MS M+ 232/234.

1. stirringThe pale mixture was stirred for a further 1 hour at -70° C.
2. customthen evaporated under vacuum
3. extractionThe residue was extracted with ether
4. customthe extract was evaporated to a pale oil which
5. customwas chromatographed on silica gel
6. washeluting with 1:1 ether

ORD-Eintrag

ord-7ce93cbe69cb4a2f939699ec8e01833a

Quelldatensatz

uspto-grants-1990_10

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US04963578