Hydrochloric Acid → HCID 178435402, compound
Reaction equation
O=[C:2]1[C:10]2[C:5](=[CH:6][C:7]([O:13][CH2:14][C:15]#[N:16])=[C:8]([Cl:12])[C:9]=2[Cl:11])[CH2:4][CH:3]1[CH2:17][CH3:18].[N-:19]=[N+:20]=[N-:21].[Na+].[Cl-].[NH4+].Cl.CN(C)C=[O:29]>>[O:29]=[C:14]([O:13][C:7]1[CH:6]=[C:5]2[C:10](=[C:9]([Cl:11])[C:8]=1[Cl:12])[CH2:2][CH:3]([CH2:17][CH3:18])[CH2:4]2)[C:15]1[NH:21][N:20]=[N:19][N:16]=1Participants
6
Procedure
A mixture of (1-oxo-2-ethyl-6,7-dichloro-5-indanyloxy)-acetonitrile (7.5 g., 0.0265 mole), sodium azide (2.02 g., 0.031 mole) and ammonium chloride (1.68 g., 0.0031 mole) in dimethylformamide (40 ml.) is heated on a steam bath for one hour and poured into dilute aqueous hydrochloric acid affording 7.3 g. (85%) of 5-(1-oxo-2-ethyl-6,7-dichloro-5-indanyloxymethyl)tetrazole which melts at 205°-206° C. after recrystallization from nitromethane.
Workup
- temperatureis heated on a steam bath for one hour
- custom(85%) of 5-(1-oxo-2-ethyl-6,7-dichloro-5-indanyloxymethyl)tetrazole which melts at 205°-206° C. after recrystallization from nitromethane
Sources & evidence
- ORD record
- ord-16f30e0fad4842f7948ecbcc512b7f46
- Source dataset
- uspto-grants-1978_01
- Patent number
- US04070539
Reaction notes
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