Allyl bromide → HCID 68835490, compound
Reaction equation
[CH3:1]OC1C=C2C(=CC=1)CC(=O)CC2.C(Br)C=C.[CH2:18]([C@:20]12[C:33]3[C:28](=[CH:29][C:30]([O:34][CH3:35])=[CH:31][CH:32]=3)[CH2:27][CH2:26][C:25]1=[CH:24][C:23](=[O:36])[CH2:22][CH2:21]2)[CH3:19]>>[CH2:18]([C@@:20]12[C:33]3[C:28](=[CH:29][C:30]([O:34][CH3:35])=[CH:31][CH:32]=3)[CH2:27][CH2:26][C:25]1=[CH:24][C:23](=[O:36])[CH2:22][CH2:21]2)[CH:19]=[CH2:1]Participants
4
Procedure
(4aR)-4a-allyl-7-methoxy-4,4a,9,10-tetrahydro-3H-phenanthren-2-one was prepared in three steps from 6-methoxy-2-tetralone and allyl bromide in a manner analogous to that described for the synthesis of (4aR)-4a-ethyl-7-methoxy-4,4a,9,10-tetrahydro-3H-phenanthren-2-one in Preparations 1a to 1c.
Sources & evidence
- ORD record
- ord-3ad77ae75e0a488aadb244df47ba7d66
- Source dataset
- uspto-grants-2009_06
- Patent number
- US07553877B2
Reaction notes
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