반응 #1328402
ord-94a152ad47834b769041e85313c6e34f
반응 방정식
용매
반응 조건
후처리
- 1여과the catalyst was filtered off
- 2기타The liquid filtrate thus obtained
- 3농축was concentrated under reduced pressure
- 4workup.ADDITIONTo the resulting residue, a saturated sodium hydrogen carbonate aqueous solution (15 ml) was added
- 5추출two 50 ml methylene chloride extractions
- 6건조The resulting organic layer was dried with anhydrous magnesium sulfate
- 7여과Magnesium sulfate was filtered off
- 8농축the liquid filtrate was concentrated under reduced pressure
실험 절차
The N,N-dibenzyl-(1R,2S,4S)-1-methyl-2-hydroxy-4-phenylhexyl amine (1.46 g, 3.77 mmol) obtained above was dissolved in methanol (25 ml). Subsequently, acetic acid (0.43 ml, 7.53 mmol) and 5% Pd-C (palladium carbon; containing 50% of water) (0.6 g) were added to the dissolved solution. This reaction solution was stirred for 16 hours at 50° C. under a hydrogen atmosphere, and the catalyst was filtered off. The liquid filtrate thus obtained was concentrated under reduced pressure. To the resulting residue, a saturated sodium hydrogen carbonate aqueous solution (15 ml) was added and two 50 ml methylene chloride extractions were performed. The resulting organic layer was dried with anhydrous magnesium sulfate. Magnesium sulfate was filtered off and the liquid filtrate was concentrated under reduced pressure to yield (1R,2S,4S)-1-methyl-2-hydroxy-4-phenylhexyl amine (0.61 g, 2.96 mmol).