Dimethylformamide diethylacetal → HCID 54306991, compound
Reaction equation
[CH3:1][C:2]1[CH:11]=[C:10]2[C:5]([CH2:6][CH2:7][CH2:8][C:9]2=[O:12])=[CH:4][CH:3]=1.C(O[CH:16](OCC)[N:17]([CH3:19])[CH3:18])C>>[CH3:16][N:17]([CH:19]=[C:8]1[CH2:7][CH2:6][C:5]2[C:10](=[CH:11][C:2]([CH3:1])=[CH:3][CH:4]=2)[C:9]1=[O:12])[CH3:18]Participants
3
Procedure
3,4-Dihydro-2-dimethylaminomethylene-7-methyl-1(2H) naphthalenone was prepared from 7-methyl-1-tetralone (4.8 g, 30 mmol) and N,N-dimethyl-formamide diethyl acetal (15.4 ml, 90 mmol). The crude product was recrystallised from diethyl ether-hexane to give yellow crystals (4.64 g) m.p. 79-82° MS (ES+) 238 (MNa+, 6%), 216 (MH+, 100%).
Workup
- customThe crude product was recrystallised from diethyl ether-hexane
Sources & evidence
- ORD record
- ord-38ea26150f144d9e81f21add8440897c
- Source dataset
- uspto-grants-2000_05
- Patent number
- US06057329
Reaction notes
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