1-Bromopentadecane → HCID 58743387, compound
Reaction equation
[CH2:1]([N:8]([C@H:16]([CH3:19])[CH:17]=[O:18])[CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Br[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH3:35]>>[CH2:9]([N:8]([C@@H:16]([C@@H:17]([OH:18])[CH2:35][CH2:34][CH2:33][CH2:32][CH2:31][CH2:30][CH2:29][CH2:28][CH2:27][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH3:21])[CH3:19])[CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1Participants
3
Procedure
According to the method of Example 26, from aldehyde 26 (445 mg, 1.76 mmol) and 1-bromopentadecane (1.28 g, 4.39 mmol), alcohol 80 was obtained as a colorless oil (422 mg, 52% yield).
Sources & evidence
- ORD record
- ord-87330289a0e04fd492ffa55ef354ebb2
- Source dataset
- uspto-grants-2006_11
- Patent number
- US07138547B2
Reaction notes
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