Hydrochloric Acid → HCID 23319739, compound
Reaction equation
[Cl:1][CH2:2][C:3]([N:5]([CH2:15][N:16]1[CH:20]=[N:19][CH:18]=[N:17]1)[C:6]1[C:11]([CH2:12][CH3:13])=[CH:10][CH:9]=[CH:8][C:7]=1[CH3:14])=[O:4].Cl>ClCCl.CCOCC>[ClH:1].[Cl:1][CH2:2][C:3]([N:5]([CH2:15][N:16]1[CH:20]=[N:19][CH:18]=[N:17]1)[C:6]1[C:11]([CH2:12][CH3:13])=[CH:10][CH:9]=[CH:8][C:7]=1[CH3:14])=[O:4]Participants
5
Procedure
10.0 parts by weight of 2-chloro-2'-methyl-6'-ethyl-N-(1,2,4-triazol-1-yl-methyl)-acetanilide is dissolved in 50 parts by volume of a mixture of anhydrous dichloromethane and ether (1:1). Dry hydrogen chloride is then passed in, while cooling, for 15 minutes, and a further 55 parts by volume of anhydrous ether is dripped in. The precipitated crystals are suction filtered, and there is obtained 7.5 parts by weight of 2-chloro-2'-methyl-6'-ethyl-N-(1,2,4-triazol-1-yl-methyl)acetanilide hydrochloride; m.p.: 148° C.
Workup
- temperaturewhile cooling, for 15 minutes
- filtrationfiltered
Sources & evidence
- ORD record
- ord-f8ecc517787f4e23ad618cb693aa637c
- Source dataset
- uspto-grants-1986_06
- Patent number
- US04593104
Reaction notes
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