HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 178527993, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 1-amino-1,2-dihydro-5H-tetrazole-5-thione | HCID 178514290 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178527993 | HCID 178527993 | 689.4% |
Reaction Steps
7.0 g of 1-amino-5-mercapto-1H-tetrazole and 0.6 g of benzaldehyde were dissolved in 120 ml of ethanol, and the solution was stirred at room temperature for 4 hours. After the reaction, the solution was evaporated to remove solvent. The residue was dissolved in 50 ml of ethyl acetate. The ethyl acetate solution was washed with water, dried and evaporated to remove solvent. Then, isopropyl ether was added to the residue obtained, and the crystalline precipitates were collected by filtration. 8.0 g of 1-benzylideneamino-5-mercapto-1H-tetrazole were obtained as colorless needles. mp 119°-120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04576938 |
| Source dataset | uspto-grants-1986_03 |
| ORD ID | ord-049119fec04c48718ce57bdab05932b0 |
| Source note | uspto-grants-1986_03 |