p-Toluenesulfonic acid → HCID 70612177, compound

Temperature

145 °C

84 g of diketene were added over 10 minutes at 10° C. to a mixture of 85 g of cyclopentylamine and 500 ml of tetrahydrofuran and after stirring the mixture for 6 hours at 20° C., the mixture was evaporated to dryness under reduced pressure. The residue was added to isopropyl ether and was cooled and vacuum filtered to obtain 107 g of N-cyclopentyl-acetylacetamide melting at 52° C. 56 g of the latter product and 1.6 g of p-toluene sulfonic acid were added to a mixture of 40 g of methyl orthoformate and 80 ml of methanol and the mixture was held at 50° C. for 8 hours and 72 hours at 25° C. 4 ml of quinoline were added and the mixture was evaporated to dryness under reduced pressure. The residue was added to toluene and the mixture was heated at 145° C. for 4 hours while distilling a toluene-methanol azeotrope. The mixture was evaporated to dryness under reduced pressure and the residue was chromatographed over silica gel. The product was eluted with an 8-2 methylene chloride-acetone mixture and was crystallized from isopropyl ether to obtain 40 g of N-cyclopentyl-3-methoxy-crotonamide melting at 94° C. The RMN spectra showed the product to be the E isomer.

1. customthe mixture was evaporated to dryness under reduced pressure
2. additionThe residue was added to toluene
3. distillationwhile distilling a toluene-methanol azeotrope
4. customThe mixture was evaporated to dryness under reduced pressure
5. customthe residue was chromatographed over silica gel
6. washThe product was eluted with an 8-2 methylene chloride-acetone mixture
7. customwas crystallized from isopropyl ether

ORD record

ord-6db95eeef96e49d0b3bfea1f249fa6c9

Source dataset

uspto-grants-1979_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04170465