HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 20484704, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cyclohexanesulfenyl chloride | HCID 87312 | — |
| Reactant | HCID 20484690 | HCID 20484690 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20484704 | HCID 20484704 | — |
Reaction Steps
7.8 grams (0.0517 mole) of cyclohexyl chlorosulfide prepared as in Example 1 is added over a 60-minute period to a stirred solution of 12 grams (0.0495 mole) of N-ethyl benzothiazole-2-sulfonamide, 5.5 grams of triethylamine (0.0495 mole) in 200 ml anhydrous dimethylformamide and 200 ml chloroform. The temperature is maintained between about 15° and 20° C. The reaction mixture is poured into 2 liters of ice water. The solvent layer is well washed, dehydrated with anhydrous sodium sulfate and any remaining solvent is removed by vacuum distillation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04410704 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-37d8412820364c6aaaa3340ed56f36c8 |
| Source note | uspto-grants-1983_10 |