Cyclopentanone → HCID 22889469, compound
Reaction equation
[C:1]1(=[O:6])[CH2:5][CH2:4][CH2:3][CH2:2]1.Cl[CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH:13]1[CH2:22][CH:21]2[CH2:23][CH:14]1[CH:15]1[CH:20]2[CH:19]2[CH2:24][CH:16]1[CH:17]=[CH:18]2>>[CH:15]12[CH:16]3[CH2:24][CH:19]([CH:18]=[CH:17]3)[CH:20]1[CH:21]1[CH2:23][CH:14]2[CH:13]([CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][C:1]2([OH:6])[CH2:5][CH2:4][CH2:3][CH2:2]2)[CH2:22]1Participants
3
Procedure
1-{5-(8-Tetracyclo[4.4.0.12,5.17,10]dodecen-3-yl)pentyl}-cyclopentanol (yield: 82%) was obtained in the same manner as in Synthesis Example 1, except that cyclopentanone and 1-chloro-5-(8-tetracyclo[4.4.0.12,5.17,10] dodecen-3-yl)pentane were used in place of acetone and 1-chloro-4-(5-norbornen-2-yl)butane, respectively.
Sources & evidence
- ORD record
- ord-938b162dc9214bf9b3f81fc1b3a05e67
- Source dataset
- uspto-grants-2002_10
- Patent number
- US06469220B2
Reaction notes
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