HuagongsheHuagongshe Chemistry Print Report · For research reference only
Epichlorohydrin → HCID 13064030, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,1,3-Benzothiadiazol-4-ol | HCID 4914673 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 13064030 | HCID 13064030 | 69% |
Reaction Steps
7.6 g (50 mM) 4-hydroxy-2,1,3-benzthiadiazole were dissolved in 100 ml. dioxan and mixed with 50 ml. epichlorohydrin and 55 ml. 1 N aqueous sodium hydroxide solution and the reaction mixture stirred for 4-5 hours at 55°-60° C. When the reaction was finished, the reaction mixture was diluted with 300 ml. water and extracted with chloroform. The dried chloroform solution was evaporated and the residue was chromatographed on a silica gel column (elution agent: chloroform). The residue obtained after evaporation of the elution fractions crystallized upon treatment with diisopropyl ether. There were obtained 7.2 g (69% of theory) 4-(2,3-epoxypropyloxy)-2,1,3-benzthiadiazole, which had a melting point of 65°-67° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04436742 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-4a7e93af69464f2bbc582b39b810da39 |
| Source note | uspto-grants-1984_03 |