1,4-Dibromobutane → 2-(5-Bromopentyl)benzo[de]isoquinoline-1,3-dione
Reaction equation
Cl.C1C2C(=CC=CC=2)CCN1CCC[CH2:15][N:16]1[C:25](=[O:26])[C:24]2[CH:27]=[CH:28][CH:29]=[C:22]3[C:23]=2[C:18](=[CH:19][CH:20]=[CH:21]3)[C:17]1=[O:30].[Br:31][CH2:32][CH2:33][CH2:34][CH2:35]CBr.BrCCCCBr>>[Br:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:15][N:16]1[C:17](=[O:30])[C:18]2[CH:19]=[CH:20][CH:21]=[C:22]3[C:23]=2[C:24](=[CH:27][CH:28]=[CH:29]3)[C:25]1=[O:26]Participants
4
Procedure
Following the procedure of part (a) of example 39 but substituting 1,5-dibromopentane for the 1,4-dibromobutane, one obtains 2-(5-bromopentyl)-1H-benz[de]isoquinoline-1,3(2H)-dione; m.p. 113°-115°.
Sources & evidence
- ORD record
- ord-0fa4267b637d4efdb46cc7471ce4e8f5
- Source dataset
- uspto-grants-1976_03
- Patent number
- US03947452
Reaction notes
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