Isobutylene → HCID 11209898, compound
Reaction equation
[CH2:1]=[C:2]([CH3:4])[CH3:3].[C:5]([C:8]12[CH2:17][CH:12]3[CH2:13][CH:14]([CH2:16][C:10]([C:18]([OH:20])=[O:19])([CH2:11]3)[CH2:9]1)[CH2:15]2)([OH:7])=[O:6]>>[C:2]([O:19][C:18]([C:10]12[CH2:16][CH:14]3[CH2:13][CH:12]([CH2:17][C:8]([C:5]([O:7][C:2]([CH3:4])([CH3:3])[CH3:1])=[O:6])([CH2:15]3)[CH2:9]1)[CH2:11]2)=[O:20])([CH3:4])([CH3:3])[CH3:1]Participants
3
Procedure
In accordance with a conventional method in which isobutene is used under acidic conditions, 10 mmol of 1,3-dicarboxyadamantane was t-butoxylated to give 1,3-di(t-butoxycarbonyl)adamantane.
Sources & evidence
- ORD record
- ord-7bec796273a74d73b5fa0fe21873a1ef
- Source dataset
- uspto-grants-2002_05
- Patent number
- US06391520B1
Reaction notes
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