HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → HCID 23347367, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Ammonium thiocyanate | HCID 15666 | — |
| Reactant | HCID 713863 | HCID 713863 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 23347367 | HCID 23347367 | — |
Reaction Steps
The starting material is obtained as follows: A solution of 6 g ammonium thiocyanate in 200 ml acetone is treated with 7 ml benzoyl chloride and stirred for 10 minutes. To this solution 6 g of 4-chloro-5-amino-2,1,3-benzothiadiazole in 200 ml of methanol is added. The mixture is boiled for 2 hours and cooled yielding N-benzoyl-N'-(4-chloro-2,1,3-benzothiadiazol-5-yl)thiourea (M.Pt. 220°-222° from methanol). The precipitate was filtered off and quickly heated to reflux with 100 ml of a 2 N aqueous solution of sodium hydroxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04217356 |
| Source dataset | uspto-grants-1980_08 |
| ORD ID | ord-9c1fffa8f3534d55aef5026b091c16ea |
| Source note | uspto-grants-1980_08 |