Benzylethanolamine → HCID 25025552, compound
Reaction equation
[CH2:1]([NH:8][CH2:9][CH2:10][OH:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:12][C:13]1[CH:21]=[CH:20][C:16]([C@H:17]2[O:19][CH2:18]2)=[CH:15][CH:14]=1>>[Cl:12][C:13]1[CH:21]=[CH:20][C:16]([C@@H:17]([OH:19])[CH2:18][N:8]([CH2:9][CH2:10][OH:11])[CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)=[CH:15][CH:14]=1Participants
3
Conditions
- Temperature
- 70 °C
Procedure
N-Benzylethanolamine (1.36 g, 1.5 equivalents) was added to (R)-4-chloro-styrene oxide (928 mg, 6.0 mmol), and the mixture was stirred at 70° C. for 3 hours. By cooling to room temperature, 2.56 g of the reaction mixture including the title compound was obtained (yield: 86%, chemical purity: 69.0 area %, N-benzyl ethanolamine: 9.2 area %, 10.4 area % of regioisomer was contaminated). The retention time in the chemical purity analysis method was 3.8 min.
Workup
- temperatureBy cooling to room temperature