Pentane → HCID 20082475, compound
Reaction equation
[ClH:1].[C:2]([O:5][CH:6]([CH2:25][N:26]([CH3:28])[CH3:27])[CH2:7][O:8][CH:9]([CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])C)(=[O:4])[CH3:3].[CH3:29][CH2:30][CH2:31]CC>>[ClH:1].[C:2]([O:5][CH:6]([CH2:25][N:26]([CH3:27])[CH3:28])[CH2:7][O:8][CH2:9][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:29][CH2:30][CH3:31])(=[O:4])[CH3:3]Participants
3
Procedure
1 l) (±)-3-dimethylamino-1-(2-hexadecyloxy)-2-propyl acetate hydrochloride; m.p. 78°-89° C. from n-pentane; yield 83.6%; and
Sources & evidence
- ORD record
- ord-80496b4ac0904f309d8e8aefcbe85291
- Source dataset
- uspto-grants-1989_08
- Patent number
- US04855489
Reaction notes
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