Butyl bromide → 1-Butylazonan-2-one
Reaction equation
[H-].[Na+].[NH:3]1[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][C:4]1=[O:12].Br[CH2:14][CH2:15][CH2:16][CH3:17]>>[CH2:14]([N:3]1[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][C:4]1=[O:12])[CH2:15][CH2:16][CH3:17]Participants
4
Procedure
Following example 10, 16.32 g of 50% sodium hydride-mineral oil dispersion (8.16 g NaH, 0.34 M), 40 g (0.283 M) of azacyclononan-2-one and 43 g (0.311 M) of 1-bromobutane was refluxed for 22 hours. The reaction mixture was diluted with benzene-tolune and was extracted with water. The organic phase was separated, dried and concentrated to a yellow oil. Distillation afforded 41.4 g (74%) of product; b.p. 166°-170°/0.2 mm.
Workup
- temperaturewas refluxed for 22 hours
- extractionwas extracted with water
- customThe organic phase was separated
- customdried
- concentrationconcentrated to a yellow oil
- distillationDistillation
Sources & evidence
- ORD record
- ord-387447f85ee5449dac9a7908c8e621e5
- Source dataset
- uspto-grants-1983_11
- Patent number
- US04415563
Reaction notes
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