Acetonitrile → HCID 53971717, compound
Reaction equation
[CH3:1][C:2]([OH:10])([CH2:4][CH2:5][CH2:6][C:7](=O)[CH3:8])[CH3:3].[OH-].[K+].[C:13](#[N:15])[CH3:14]>>[CH3:8][C:7]1([CH2:14][C:13]#[N:15])[CH2:6][CH2:5][CH2:4][C:2]([CH3:1])([CH3:3])[O:10]1Participants
4
Procedure
The distillation residue of the second reaction is again recycled for a third synthesis after adding a further 122.7 g of 94.5% 2-methyl-heptan-2-ol-6-one (0.80525 moles), 5.2853 g of 86% KOH and acetonitrile in the usual ratio. After the reaction, distillation gives 82.0 g of 2,6,6-trimethyl-2-cyanomethyltetrahydropyran (0.49099 moles) in the distillate, together with the unconverted hydroxyketone.
Workup
- customThe distillation residue of the second reaction
- customis again recycled for a third synthesis
- customAfter the reaction, distillation
Sources & evidence
- ORD record
- ord-268c091508c74b48a1ba7e4d406dab9c
- Source dataset
- uspto-grants-1981_07
- Patent number
- US04278602
Reaction notes
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