Butanal → HCID 70588461, compound
Reaction equation
[CH:1](=O)[CH2:2][CH2:3][CH3:4].[CH:6]1([NH2:12])[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1.S([O-])([O-])(=O)=O.[Na+].[Na+]>>[CH:1](=[C:7]1[CH2:8][CH2:9][CH2:10][CH2:11][CH:6]1[NH2:12])[CH2:2][CH2:3][CH3:4]Participants
4
Procedure
At 0° C., 16.3 g (20 mL, 0.23 mol) of butyraldehyde (Formula IV) was added dropwise to 21.7 g (25 mL, 0.22 mol) of cyclohexylamine (Formula III). After 1 h, 6 g of anhydrous sodium sulfate was added and the mixture stirred for 5 h. The product was decanted from the salt water slurry, dried by addition of further 10 g of anhydrous sodium sulfate, filtered and distilled. Characteristics of the product: bp 88° C. (20 mm); yield 86%; NMR (CDCl3, δ): 1.0 (3H, t) 1.1-2.1 (12H), 2.3 (2H, g), 3.0 (1H, m), 7.8 (1H, t).
Workup
- customThe product was decanted from the salt water slurry
- dry with materialdried by addition of further 10 g of anhydrous sodium sulfate
- filtrationfiltered
- distillationdistilled
Sources & evidence
- ORD record
- ord-5176bc7b717446ac88b809a2854aef31
- Source dataset
- uspto-grants-1980_09
- Patent number
- US04220774
Reaction notes
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