Acrylonitrile → HCID 10420903, compound
Reaction equation
[CH:1]([O:4][P:5]([C:7]([CH3:10])([CH3:9])[CH3:8])[OH:6])([CH3:3])[CH3:2].[Na].[C:12](#[N:15])[CH:13]=[CH2:14]>>[C:12]([CH2:13][CH2:14][P:5]([C:7]([CH3:10])([CH3:9])[CH3:8])(=[O:6])[O:4][CH:1]([CH3:3])[CH3:2])#[N:15]Participants
4
Procedure
To 15.7 g of t-butylphosphonous acid-isopropylester in 6.3 ml of acrylonitrile are added 21 ml of sodium isopropylate (0.25 molar). After the exothermic reaction (the temperature rises to 100°) the suspension is filtered, the filtrate evaporated and the residue distillated to yield isopropyl 2-cyanoethyl(t-butyl)phosphinate as an oil,b.p. 121°/8 Pa, nD20 =1.4480.
Workup
- customAfter the exothermic reaction (the temperature
- customrises to 100°
- filtrationis filtered
- customthe filtrate evaporated
Sources & evidence
- ORD record
- ord-8aa727bdfc6346d7ba7b2664d2613aed
- Source dataset
- uspto-grants-1991_09
- Patent number
- US05051524
Reaction notes
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