Benzenepropanal → HCID 13105329, compound

A stirred suspension of sodium hydride (12.0 g, 50% dispersion in oil) in dry dimethyl sulphoxide (100 ml) was heated to 70° to 75° C. under nitrogen for 40 minutes. The dark solution was cooled, a solution of 4-carboxybutyltriphenylphosphonium bromide (53 g) in dry dimethyl sulphoxide (100 ml) was added over 20 minutes at 20° to 25° C., and the solution was stirred for a further 10 minutes. 3-Phenyl-propionaldehyde (12.5 ml) was added with cooling to maintain a temperature of 30° to 35° C. and the mixture was stirred for a further 4 hours at room temperature, then poured on to ice-water (600 ml) and washed with chloroform. The aqueous phase was acidified and extracted with chloroform. The extract was washed with water, dried, and evaporated. The residual oil was distilled under vacuum to give the above product, b.p. 134° to 139° C./0.07 mm. 13C NMR spectroscopy showed the presence of about 5% (E)-isomer.

1. temperaturewas heated to 70° to 75° C. under nitrogen for 40 minutes
2. temperatureThe dark solution was cooled
3. temperaturewith cooling
4. temperatureto maintain a temperature of 30° to 35° C.
5. stirringthe mixture was stirred for a further 4 hours at room temperature
6. washwashed with chloroform
7. extractionextracted with chloroform
8. washThe extract was washed with water
9. customdried
10. customevaporated
11. distillationThe residual oil was distilled under vacuum
12. customto give the above product, b.p. 134° to 139° C./0.07 mm

ORD record

ord-cae47b400d354ee083eb1e53e1545e59

Source dataset

uspto-grants-1985_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04513005