ethyl (+/-)-5-decyl-alpha-phenyl-2H-tetrazole-2-acetate → 5-dodecyl-alpha-(1-methylethyl)-2H-tetrazole-2-acetic acid
Reaction equation
[CH2:1]([C:13]1[N:14]=[N:15][N:16]([CH:18]([CH:24]([CH3:26])[CH3:25])[C:19]([O:21]CC)=[O:20])[N:17]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].C(C1N=NN(C(C2C=CC=CC=2)C(OCC)=O)N=1)CCCCCCCCC>>[CH2:1]([C:13]1[N:14]=[N:15][N:16]([CH:18]([CH:24]([CH3:25])[CH3:26])[C:19]([OH:21])=[O:20])[N:17]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]Participants
3
Procedure
When in the general procedure of Example 79 an appropriate amount of ethyl (±)-5-dodecyl-α-(1-methylethyl)-2H-tetrazole-2-acetate was substituted for ethyl (±)-5-decyl-α-phenyl-2H-tetrazole-2-acetate, the title compound was obtained, mp 39°-42° C.
Sources & evidence
- ORD record
- ord-50f3cca5ca274fc1bce83e01f4502f83
- Source dataset
- uspto-grants-1995_08
- Patent number
- US05441975
Reaction notes
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