Hexadecanolide → N-methoxy-N-methyl-16-hydroxyhexadecanamide

温度

-78 °C

1.78 g of dimethylhydroxylamine (17.687 mmol; 3 eq.; MW=97.55) were dissolved in 10 mL of CH2Cl2 that had been distilled under argon and cooled to −78° C. 8.8 mL of AlMe3, 2M in hexane, (17.687 mmol; 3 eq.; MW=72.09) were added drop by drop at −78° C. and the reaction mixture was stirred at room temperature for half an hour. The solution was then cooled down to 0° C. and 1.55 g of oxacycloheptadecan-2-one (5.895 mmol; 1 eq.; MW=254.42), dissolved in 5 mL of distilled CH2Cl2, were added drop by drop. The reaction mixture was left at room temperature under stirring. Thin layer chromatographical analysis showed that the reaction was completed after one hour and a half. The solution was added dropwise into a mixture of 60 mL of Et2O/MeOH 2:1 cooled to −78° C. and then filtered over celite. 100 mL of a saturated, aqueous solution of NaHCO3 were added and the aqueous phase was extracted with ether. The organic phases were combined, dried over magnesium sulfate and then evaporated under reduced pressure to afford 1.66 g of N-methoxy-N-methyl-16-hydroxyhexadecanamide, corresponding to 5.262 mmol and a yield of 89%. The amide obtained in this way was subsequently used without any additional purification.

1. distillationhad been distilled under argon
2. addition8.8 mL of AlMe3, 2M in hexane, (17.687 mmol; 3 eq.; MW=72.09) were added drop by drop at −78° C.
3. temperatureThe solution was then cooled down to 0° C.
4. additionwere added drop by drop
5. waitThe reaction mixture was left at room temperature
6. stirringunder stirring
7. temperaturecooled to −78° C.
8. filtrationfiltered over celite
9. addition100 mL of a saturated, aqueous solution of NaHCO3 were added
10. extractionthe aqueous phase was extracted with ether
11. dry with materialdried over magnesium sulfate
12. customevaporated under reduced pressure

ORDレコード

ord-aacd5194daa846498c4babcd585515f5

出典データセット

uspto-grants-2010_04

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07691900B2