2-Methyldodecanoic acid → 2,2-Dimethyldodecanoyl chloride
Reaction equation
[CH3:1][CH:2]([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15])[C:3]([Cl:5])=[O:4].[CH3:16]C(CCCCCCCCCC)C(O)=O>>[CH3:1][C:2]([CH3:16])([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH3:15])[C:3]([Cl:5])=[O:4]Participants
3
Procedure
In a similar manner to that described in Example 25 except for the use of 2-methyldodecanoyl chloride [synthesized by chlorinating 2-methyldodecanoic acid which was synthesized by the process described in Organic Synthesis, 4,616, by the method as described in B. D. Roth. et al., Journal of Medicinal Chemistry, 35, 1609-1617 (1992)] instead of 2,2-dimethyldodecanoyl chloride, 82.5 mg of the desired compound was obtained as a white powder.
Workup
- customsynthesized
- customwas synthesized by the process
- customdescribed in Organic Synthesis, 4,616, by the method
Sources & evidence
- ORD record
- ord-6a990363e33945e4a3a65b4b4acc235c
- Source dataset
- uspto-grants-2002_10
- Patent number
- US06472384B1
Reaction notes
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