Hydrochloric Acid → HCID 178479233, compound
Reaction equation
C([NH:4][CH2:5][CH2:6][N:7]1[C:11](=[S:12])[NH:10][N:9]=[N:8]1)(=O)C.[ClH:13]>>[ClH:13].[NH2:4][CH2:5][CH2:6][N:7]1[C:11](=[S:12])[NH:10][N:9]=[N:8]1Participants
3
Procedure
A mixture of 21.5 g. (11.4 mmol) of 1-[2-(acetylamino)ethyl]-1,4-dihydro-5H-tetrazole-5-thione in 300 ml. of 6N hydrochloric acid was heated at reflux for 3.5 hours. The mixture was filtered after cooling to room temperature. The filtrate was concentrated to small volume. The residual liquid was diluted with i-propanol. The solid which precipitated was filtered, washed and dried in vacuo to give 13.7 g. of 1-(2-aminoethyl)-1,4-dihydro-5H-tetrazole-5-thione, hydrochloride (66.1% yield) mp 232°-233.5° C.
Workup
- additionA mixture of 21.5 g
- temperatureat reflux for 3.5 hours
- filtrationThe mixture was filtered
- concentrationThe filtrate was concentrated to small volume
- additionThe residual liquid was diluted with i-propanol
- customThe solid which precipitated
- filtrationwas filtered
- washwashed
- customdried in vacuo
- customto give 13.7 g
Sources & evidence
- ORD record
- ord-25819c90047e42fca256641ba95a3411
- Source dataset
- uspto-grants-1978_09
- Patent number
- US04117125
Reaction notes
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