HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 20215696, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Butyl isocyanate | HCID 8110 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 14774740 | HCID 14774740 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 20215696 | HCID 20215696 | — |
Reaction Steps
To 140 mL of methyl ethyl ketone was added 14.3 g of 3-chloro-N,N-dimethyl-1,2-benzenedisulfonamide, 7.2 g of potassium carbonate and 7.5 ml of n-butyl isocyanate. This mixture was heated at reflux temperature for 3 hours, cooled to room temperature, poured into 1500 mL of ice water, and acidified to pH 1 with concentrated hydrochloric acid. The resulting precipitate was collected, washed with water, and dried to afford 17.4 g of N'-butylaminocarbonyl-3-chloro-N,N-dimethyl-1,2-benzenedisulfonamide as a white powder, m.p. 107°-115° C.; NMR (CDCl3): δ0.9 (br t, 3H), 1.2-1.7 (m, 4H), 3.0 (s, 6H), 3.3-3.4 (m, 2H), 6.6 (t, 1H), 7.6-8.0 (m, 2H), 8.5 (dd, 1H), 9.0 (br s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04645527 |
| Source dataset | uspto-grants-1987_02 |
| ORD ID | ord-a03d04f283604985a697b95fae5b3697 |
| Source note | uspto-grants-1987_02 |