Benzaldehyde → (S)-2-(Benzylideneamino)-3-methylbutan-1-ol
Reaction equation
[CH:1](=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:9][C@H:10]([CH2:14][OH:15])[CH:11]([CH3:13])[CH3:12]>C1(C)C=CC=CC=1>[CH3:12][CH:11]([CH3:13])[C@H:10]([N:9]=[CH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)[CH2:14][OH:15]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2.64 ml (2.78 g, 26.16 mmol) of benzaldehyde were added to a stirred solution of 2.57 g (24.91 mmol) of L-valinol in 28 ml of toluene, and the mixture was heated under reflux with a water trap for one hour. Cooling was followed by concentration and recrystallization from heptane. The colorless solid was filtered off with suction and dried under reduced pressure (3.74 g).
Workup
- temperaturethe mixture was heated
- temperatureunder reflux with a water trap for one hour
- temperatureCooling
- concentrationwas followed by concentration and recrystallization from heptane
- filtrationThe colorless solid was filtered off with suction
- customdried under reduced pressure (3.74 g)
Sources & evidence
- ORD record
- ord-d5e4786a78714b6888238efaf79180f8
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08580777B2
Reaction notes
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