Hydrochloric Acid → HCID 21564731, compound
Reaction equation
[OH:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH2:4][CH2:5][CH2:6][C:7]2=[O:12].Cl[CH2:14][CH2:15][CH2:16][N:17]1[CH2:22][CH2:21][N:20]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=2[CH2:29][CH3:30])[CH2:19][CH2:18]1.Cl>>[CH2:29]([C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=1[N:20]1[CH2:21][CH2:22][N:17]([CH2:16][CH2:15][CH2:14][O:1][C:2]2[CH:11]=[CH:10][CH:9]=[C:8]3[C:3]=2[CH2:4][CH2:5][CH2:6][C:7]3=[O:12])[CH2:18][CH2:19]1)[CH3:30]Participants
4
Procedure
from 5-hydroxy-1-oxotetraline and 1-(3-chloropropyl)-4-(2-ethylphenyl)-piperazine; yield 70% of theory; m.p. of the hydrochloride (recrystallized from water) 209°-210°C;
Sources & evidence
- ORD record
- ord-4143bd9b2424458b9bcef85294094a4b
- Source dataset
- uspto-grants-1976_01
- Patent number
- US03932411
Reaction notes
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