HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl isocyanate → 2-(Chloromethyl)-N-(butylaminocarbonyl)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl isocyanate | HCID 8110 | — |
| Reactant | 2-(Chloromethyl)benzenesulfonamide | HCID 13364627 | — |
| Catalyst | Diazabicyclo(2.2.2)octane | HCID 136165 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2-(Chloromethyl)-N-(butylaminocarbonyl)benzenesulfonamide | HCID 13631887 | 74.8% |
Reaction Steps
A mixtue of 2-(chloromethyl)benzenesulfonamide (13.2 g, 64 mmol) and butyl isocyanate (7.0 g, 71 mmol) in xylene (80 ml) was contacted with diazabicyclo[2.2.2]-octane (0.25 g) and heated to reflux for 5.0 hrs. Volatiles were removed under vacuum and the residue was treated with 0.5N NaOH (200 ml) and extracted with ethyl acetate (75 ml). The aqueous layer was separated, chilled, acidified (pH 4) with hydrochloric acid, and extracted with ethyl acetate. The organic layer was washed with brine, dried (MgSO4), and evaporated to give 14.6 g of white solid. A sample was recrystallized from toluene to give m.p. 104°-106°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04586952 |
| Source dataset | uspto-grants-1986_05 |
| ORD ID | ord-201b00dd50774394a1d639d4e156cb20 |
| Source note | uspto-grants-1986_05 |