HCID 18423026, compound → HCID 53910814, compound

A solution (220 ml) of (+)-4-(1-acetamidoethyl)benzoic acid (51.2 g) and 5% ruthenium carbon (35.4 g) in 28% aqueous ammonia was stirred in an autoclave at initial hydrogen pressure of 70 atm and at 90° C. for 3 hours and then at 150° C. for 3 hours. After completion of the reaction, the catalyst was filtered off and the filtrate was concentrated under reduced pressure to give 53.5 g of a cis- and trans- mixture of (+)-4-(1-acetamidoethyl)cyclohexanecarboxylic acid. Then, a solution of 31% hydrochloric acid-methanol (33 ml) and methanol (200 ml) were added thereto and the mixture was refluxed for 4 hours. After completion of the reaction, the mixture was concentrated under reduced pressure and the residue obtained was poured into ice water and extracted with chloroform. The extract was washed with water, dried and concentrated under reduced pressure. The residue obtained was purified by silica gel column chromatography to give 38.0 g of a cis- and transmixture (2:1) of methyl (+)-4-(1-acetamidoethyl)cyclohexanecarboxylate. [α]D =+11.4° (methanol, c=1)

1. customAfter completion of the reaction
2. filtrationthe catalyst was filtered off
3. concentrationthe filtrate was concentrated under reduced pressure
4. customto give
5. temperaturethe mixture was refluxed for 4 hours
6. customAfter completion of the reaction
7. concentrationthe mixture was concentrated under reduced pressure
8. customthe residue obtained
9. extractionextracted with chloroform
10. washThe extract was washed with water
11. customdried
12. concentrationconcentrated under reduced pressure
13. customThe residue obtained
14. customwas purified by silica gel column chromatography

ORD record

ord-ba6cc26283b940268f0b47d126e53604

Source dataset

uspto-grants-1995_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05478838