HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 131710862, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Chlorobenzenesulfenylchloride | HCID 11084465 | — |
| Reactant | HCID 88816106 | HCID 88816106 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131710862 | HCID 131710862 | — |
Reaction Steps
A 2.2 g (0.012 mol) sample of p-chlorophenylsulfenyl chloride was added dropwise to a cooled (-5° C. to 0° C.) solution of 3.5 g (0.1 mol) 4-ethylpropylamino-N-methyl-3,5-dinitrobenzenesulfonamide and 1.1 g (0.014 mol) pyridine in 25 ml dichloromethane. The reaction was stirred for 20 minutes and then diluted with 50 ml dichloromethane, washed with water, washed with aqueous sodium bicarbonate solution, and dried over magnesium sulfate. The dichloromethane was then evaporated under reduced pressure to give a solid residue. Recrystallization from ethanol gave the product as red-orange plates, m.p. 89°-91° C. Elemental analysis for C18H21ClN4O6S2 showed: % S, calc. 13.1, found 13.3; % Cl, calc. 7.3, found 7.8.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04041159 |
| Source dataset | uspto-grants-1977_08 |
| ORD ID | ord-de8259e0ee274f85aa6f51b5723aa10f |
| Source note | uspto-grants-1977_08 |