反应 #2200587

反应方程式

(S)-(−)-1-phenylethylamine

(2S,3S)-2-methyl-3-tetrahydropyranyloxybutyraldehyde

(2S,3S)-2-methyl-3-benzyloxybutyraldehyde

methanol

TMSCN

→

(1R,2R,3S)-1-cyano-2-methyl-3-tetrahydropyranyloxy-N-[(S)-1′-phenylethyl]butylamine

(1S,2R,3S)-1-cyano-2-methyl-3-tetrahydropyranyloxy-N-[(S)-1′-phenylethyl]butylamine

收率 90.0%

溶剂

dichloromethane

反应条件

后处理

1. 1
   workup.WAITat room temperature for 22 hours
2. 2
   其他the reaction mixture was separated in saturated NaHCO3
3. 3
   萃取The aqueous phase was extracted with ether
4. 4
   洗涤the ether extracts were washed with brine, they
5. 5
   其他were dried
6. 6
   过滤filtered on a short disk of Celite and Na2SO4

实验过程

(S)-(−)-1-phenylethylamine (211 mg, 225 μl, 1.74 mmol) was added at room temperature to a solution of (2S,3S)-2-methyl-3-tetrahydropyranyloxybutyraldehyde (6) (270 mg, 1.45 mmol) in dichloromethane (6 ml), and the stirring was continued at room temperature for 2 hours. The reaction mixture was cooled to 0° C., and methanol (2 ml) and TMSCN (216 mg, 290 μl, 2.18 mmol) were successively introduced. After stirring at 0° C. for 2 hours and then at room temperature for 22 hours, the reaction mixture was separated in saturated NaHCO3 and ether. The aqueous phase was extracted with ether, the ether extracts were washed with brine, they were dried and filtered on a short disk of Celite and Na2SO4 and then evaported. Flash chromatography on a silica gel column with, as eluent, a heptane/EtOAc=10:1 then 8:1 mixture produced (1R,2R,3S)-1-cyano-2-methyl-3-tetrahydropyranyloxy-N-[(S)-1′-phenylethyl]butylamine (1R)-(17) and (1S,2R,3S)-1-cyano-2-methyl-3-tetrahydropyranyloxy-N-[(S)-1′-phenylethyl]butylamine (1S)-(17) (414 mg in total, 90%) in the ratio of about 1:3.

来源