Hydrogen Bromide → HCID 13125066, compound
Reaction equation
[CH:1]1([C:7]([CH:9]2[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]2)=O)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH:15]1([Mg]Br)[CH2:17][CH2:16]1.CO.[BrH:22]>O1CCCC1.C(O)(=O)C>[CH:1]1([C:7]([CH:9]2[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]2)=[CH:16][CH2:15][CH2:17][Br:22])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
Following the procedures of Example 15, 9.7 g. (0.05 mole) of dicyclohexyl ketone and 14.4 g. (0.1 mole) of cyclopropyl magnesium bromide in dry tetrahydrofuran were reacted and the resulting carbinol dissolved in glacial acetic acid was treated with hydrogen bromide to give 4,4-dicyclohexyl-3-butenyl bromide, b.p. 168°-171° C. (0.1 mm.).
Sources & evidence
- ORD record
- ord-35e088ee462e4a7bb2c43e4d4305b931
- Source dataset
- uspto-grants-1983_05
- Patent number
- US04383999
Reaction notes
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