Nonanoic acid, 9-hydroxy-, methyl ester → HCID 5326972, compound

8-Methoxycarbonyl-1-octanol (21.4 g, 0.115 mole) and dried mercuric cyanide (30.3 g, 0.119 mole) were dissolved in a 1:1 mixture of dry distilled benzene-nitromethane (850 ml). The solution was stirred and 200 ml of solvent was distilled. Mixed solvent (200 ml) was added and calcium sulfate (40 g) was added followed by 2,3,4,6-tetra-O-acetyl-α-D-galactosyl bromide (38.7 g, 0.094 mole). The mixture was stirred at room temperature for 36 h and then heated at 70° for 2 h. After cooling, the solution was filtered and the filtrate evaporated in vacuo to give a yellow syrup. This syrup was dissolved in distilled ethyl acetate (500 ml) and the solution was washed with an aqueous solution (10% w/w, 500 ml) of sodium iodide. The organic phase was then washed successively with a saturated solution of sodium thiosulphate (200 ml) and H2O (2×250 ml). The organic phase was dried over sodium sulphate and then evaporated in vacuo after filtration. This syrup (~50 g) after drying under high vacuum overnight was dissolved in dry distilled methanol (200 ml) and to this solution, 200 ml of methanolic sodium methoxide (150 mg of sodium) was added. After stirring at room temperature for 24 h, acid resin (prewashed a few times in methanol) was added and stirred until the pH was neutral. After filtration, the solution was evaporated and the waxy residue dissolved at room temperature in 100 ml of H2O. This solution was extracted with ether (2×40 ml) and then placed in the fridge. Upon standing, crystallization occurred. The white crystals were filtered and dried. Weight 13.5 g (41%), mp 104°-105°, [α]D25 -13.4° (c 1, 95% ethanol).

1. customof dry
2. distillationdistilled benzene-nitromethane (850 ml)
3. distillation200 ml of solvent was distilled
4. additionMixed solvent (200 ml) was added
5. additioncalcium sulfate (40 g) was added
6. stirringThe mixture was stirred at room temperature for 36 h
7. temperatureheated at 70° for 2 h
8. temperatureAfter cooling
9. filtrationthe solution was filtered
10. customthe filtrate evaporated in vacuo
11. customto give a yellow syrup
12. washthe solution was washed with an aqueous solution (10% w/w, 500 ml) of sodium iodide
13. washThe organic phase was then washed successively with a saturated solution of sodium thiosulphate (200 ml) and H2O (2×250 ml)
14. dry with materialThe organic phase was dried over sodium sulphate
15. customevaporated in vacuo
16. filtrationafter filtration
17. dry with materialThis syrup (~50 g) after drying under high vacuum overnight
18. dissolutionwas dissolved
19. customin dry
20. distillationdistilled methanol (200 ml)
21. additionto this solution, 200 ml of methanolic sodium methoxide (150 mg of sodium) was added
22. stirringAfter stirring at room temperature for 24 h
23. additionwas added
24. stirringstirred until the pH
25. filtrationAfter filtration
26. customthe solution was evaporated
27. dissolutionthe waxy residue dissolved at room temperature in 100 ml of H2O
28. extractionThis solution was extracted with ether (2×40 ml)
29. customcrystallization
30. filtrationThe white crystals were filtered
31. customdried

ORD record

ord-6a8daa4fe6514ae68d7b50982fbb92fd

Source dataset

uspto-grants-1980_12

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US04238473