HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 53819561, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cinnamyl Alcohol | HCID 5315892 | — |
| Reactant | 1,2,3-Benzothiadiazole-7-carbonyl chloride | HCID 18377607 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53819561 | HCID 53819561 | — |
Reaction Steps
3 g of benzo-1,2,3-thiadiazole-7-carboxylic acid chloride in 25 ml of dichloromethane are added dropwise at 15° C., with cooling and stirring, to a solution of 2.3 g of cinnamic alcohol, 3.5 g of triethylamine and a spatula tip of 4-dimethylaminopyridine in 13 ml of dichloromethane, the mixture is stirred for 16 hours at room temperature, ice-water is added, and the aqueous phase is extracted with dichloromethane. The extracts are washed with water, dried over Na2SO4 and concentrated by evaporation. The solid residue is triturated with a small amount of diethyl ether, yielding the title compound with a melting point of 70°-72° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05302607 |
| Source dataset | uspto-grants-1994_04 |
| ORD ID | ord-09b71fe41a0b485f8786ab6f98454ec5 |
| Source note | uspto-grants-1994_04 |