4-(Adamantan-1-ylmethoxy)-3-bromobenzonitrile → 4-(Adamantan-2-ylmethoxy)-3-cyclopropylbenzonitrile
Reaction equation
[C:1]12([CH2:11]OC3C=CC(C#N)=CC=3Br)CC3CC(CC(C3)[CH2:2]1)C2.[CH:22]12[CH2:31][CH:26]3[CH2:27][CH:28]([CH2:30][CH:24]([CH2:25]3)[CH:23]1[CH2:32][O:33][C:34]1[CH:41]=[CH:40][C:37]([C:38]#[N:39])=[CH:36][C:35]=1Br)[CH2:29]2>>[CH:22]12[CH2:31][CH:26]3[CH2:27][CH:28]([CH2:30][CH:24]([CH2:25]3)[CH:23]1[CH2:32][O:33][C:34]1[CH:41]=[CH:40][C:37]([C:38]#[N:39])=[CH:36][C:35]=1[CH:11]1[CH2:1][CH2:2]1)[CH2:29]2Participants
3
Procedure
Following the procedure as described in Example 39 step 1 and making variation as required to replace 4-(adamantan-1-ylmethoxy)-3-bromobenzonitrile with 4-(adamantan-2-ylmethoxy)-3-bromobenzonitrile the title compound was obtained as a colorless solid (0.68 g, 84%): MS (ES+) m/z 308.3 (M+1).
Sources & evidence
- ORD record
- ord-083ddc6d0cf845e1aa8598775e99d145
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08952169B2
Reaction notes
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