Chloride → HCID 86688832, compound
Reaction equation
[C:1]([OH:6])(=[O:5])[CH2:2][CH2:3][CH3:4].[C:7]([O:23][CH2:24][CH3:25])(=[O:22])[CH2:8][C:9]([CH2:16][C:17]([O:19][CH2:20][CH3:21])=[O:18])([C:11]([O:13][CH2:14][CH3:15])=[O:12])[OH:10].[Cl-]>>[C:1]([OH:6])(=[O:5])[CH2:2][CH2:3][CH2:4][CH2:7][CH2:8][CH2:9][CH2:16][CH2:17][CH2:17][CH2:16][CH2:9][CH2:8][CH3:7].[C:17]([O:19][CH2:20][CH3:21])(=[O:18])[CH2:16][C:9]([CH2:8][C:7]([O:23][CH2:24][CH3:25])=[O:22])([C:11]([O:13][CH2:14][CH3:15])=[O:12])[OH:10]Participants
3
Procedure
The same procedure was used as for preparation of triethyl citrate butyrate but using myristryl chloride.
Sources & evidence
- ORD record
- ord-64fcd8f808644030b0ece51bc9e7930f
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09127232B2
Reaction notes
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