Stearoyl chloride → Dodecanoyl chloride
Reaction equation
CC1N(CCC2CCNCC2)C=CN=1.[C:15]([Cl:34])(=[O:33])[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26]CCCCCC>>[C:15]([Cl:34])(=[O:33])[CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]Participants
3
Procedure
Following essentially the last step of the procedure for preparing the compound of Example 1, and using in place of stearoyl chloride, an approximately equivalent amount of dodecanoyl chloride, a solid was obtained.
Sources & evidence
- ORD record
- ord-4bf7382b4a204e1ca683ccf03d166ad5
- Source dataset
- uspto-grants-1990_05
- Patent number
- US04925851
Reaction notes
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