Ammonia → HCID 86674767, compound
Reaction equation
[CH3:1][C:2]1([CH3:9])[CH2:7][CH2:6][CH2:5][C:4](=O)[CH2:3]1.[C:10]([O:14]C)(=O)[C:11]#[CH:12].[NH3:16]>>[CH3:1][C:2]1([CH3:9])[CH2:3][C:4]2[NH:16][C:10](=[O:14])[CH:11]=[CH:12][C:5]=2[CH2:6][CH2:7]1Participants
4
Conditions
- Temperature
- 140 °C
Procedure
A solution of 3,3-dimethylcyclohexanone (10 g, 71.3 mmol) and methyl propiolate (11.5 g, 136 mmol) in ammonia (390 ml, 2.73 mol) was heated and stirred in an autoclave at 140° C. for 16 h. The autoclave was cooled to ambient temperature, and the reaction mixture was transferred into a 1 L round-bottomed flask and was evaporated in vacuo to give a solid residue which was purified by gradient chromatography on silica with ethyl acetate in heptane to give 7.0 g (55%) of the title compound as colorless oil; LC-MS (UV peak area/EIC) 85%, 178.1228 (M+H)+.
Workup
- temperatureThe autoclave was cooled to ambient temperature
- customthe reaction mixture was transferred into a 1 L round-bottomed flask
- customwas evaporated in vacuo
- customto give a solid residue which
- customwas purified by gradient chromatography on silica with ethyl acetate in heptane
Sources & evidence
- ORD record
- ord-9f2f37b0c8e2419d816b77d45d6f2ed7
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09321727B2
Reaction notes
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