Acetaldehyde → HCID 89525575, compound
Reaction equation
C[C:2]1[CH:3]([C:11](=O)C)[CH2:4][CH:5]2[CH:7]([CH:8]=1)[C:6]2([CH3:10])[CH3:9].[CH:14](=[O:16])[CH3:15].B(F)(F)F.[CH3:21][CH2:22][O:23]CC>ClCCCl>[C:14]([O:23][C@H:22]([C@@H:4]1[C:3]([CH3:11])=[CH:2][CH2:8][C@@H:7]2[C@H:5]1[C:6]2([CH3:9])[CH3:10])[CH3:21])(=[O:16])[CH3:15]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Following the general procedure as described in Example 1, 1-(4,7,7-trimethylbicyclo[4.1.0]hept-4-en-3-yl)ethanone (1.78 g, 10 mmol), acetaldehyde (0.53 g, 12 mmol) and boron trifluoride etherate (0.14 g, 1.0 mmol) in 1,2-dichloroethane (10 mL) were reacted to give the title product as a colorless liquid (1.82 g, 82% yield).
Workup
- customwere reacted
Sources & evidence
- ORD record
- ord-387d9fbbe9ec448e910210f045ce9721
- Source dataset
- uspto-grants-2016_06
- Patent number
- US09371262B2
Reaction notes
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