1-Bromododecane → (2S,3R)-2-(N,N-Dibenzylamino)-3-pentadecanol
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][CH3:32]>>[CH2:9]([N:8]([C@H:16]([C@H:17]([OH:18])[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 4 (273 mg, 1.08 mmol) and 1-bromododecane (671 mg, 2.69 mmol), alcohol 31 was obtained as a colorless oil (195 mg, 43% yield).
Sources & evidence
- ORD record
- ord-fc36ce42b5d7465ca9d5115322540afc
- Source dataset
- uspto-grants-2006_11
- Patent number
- US07138547B2
Reaction notes
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