HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiobenzamide → HCID 15458851, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiobenzamide | HCID 683563 | — |
| Reactant | HCID 18347149 | HCID 18347149 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15458851 | HCID 15458851 | — |
Reaction Steps
0.3 g of 2,7-dibromo-3,4-dihydro-2H-naphthalen-1-one is dissolved in 10 ml of ethanol and, after addition of 140 mg of thiobenzamide, heated to reflux for 5 h. The reaction mixture is concentrated in vacuo, the residue is suspended in 10 ml of 1 N sodium hydroxide solution and stirred at room temperature for 1 h. The suspension is filtered with suction, thoroughly washed with water and dried in vacuo. 8-Bromo-2-phenyl-4,5-dihydro-naphtho[1,2-d]thiazole is obtained with a melting point of 85° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06329407B1 |
| Source dataset | uspto-grants-2001_12 |
| ORD ID | ord-d3e092af80bd44df9c65fef00df7263d |
| Source note | uspto-grants-2001_12 |