Hydrochloric Acid → HCID 178525857, compound
Reaction equation
C([O:3][C:4](=[O:12])[CH2:5][N:6]1[C:10](Cl)=[N:9][N:8]=[N:7]1)C.NC(N)=[S:15].O.Cl>C(O)C>[SH:15][C:10]1[N:6]([CH2:5][C:4]([OH:3])=[O:12])[N:7]=[N:8][N:9]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
In a 500 ml round flash equipped with agitator, relux condenser, thermometer and a dropping funnel a mixture of 100 g (0.52 mol) 5-Chloro-1H-tetrazole-1-acetic acid ethyl ester, 44 g (0,57 Mol) thiourea, 210 g water and 25 g of 38 wt.% aqueous hydrochloric acid was heated to reflux for 6 hours, while the ethanol formed during the reaction was distilled off. For working up purpose, the residue was extracted with methyl isobutyl ketone. After evaporation of the ketone 57.9 g=69% of the theory of a white crystalline solid (melting point 173° C.) of 5-Mercapto-1H-tetrazole-1-acetic acid was obtained (purity 99%).
Workup
- customIn a 500 ml round flash equipped with agitator, relux condenser
- temperaturewas heated
- customformed during the reaction
- distillationwas distilled off
- extractionthe residue was extracted with methyl isobutyl ketone
- customAfter evaporation of the ketone 57.9 g=69% of the theory of a white crystalline solid (melting point 173° C.) of 5-Mercapto-1H-tetrazole-1-acetic acid
- customwas obtained (purity 99%)
Sources & evidence
- ORD record
- ord-4a0ee8bf7b934a50ae3f5ac7a7555d7c
- Source dataset
- uspto-grants-1987_03
- Patent number
- US04652671
Reaction notes
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