HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosulfonyl isocyanate → 2,6-Bis(1-methylethyl)-4-nitrophenyl sulfamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | 2,6-Diisopropyl-4-nitrophenol | HCID 10680603 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,6-Bis(1-methylethyl)-4-nitrophenyl sulfamate | HCID 18698845 | 60% |
Reaction Steps
N-Chlorosulfonyl isocyanate (7.2 mL, 82.6 mmol) was added slowly to a warm solution of 2,6-bis(1-methylethyl)-4-nitrophenol (17.57 g, 78.7 mmol) in 400 mL toluene. The resulting solution was heated to reflux for 6 hours and then cooled to room temperature and concentrated to give a brown oil. Quenched with 200 g ice and extracted with 4×500 mL dichloromethane. The organic solution was dried over MgSO4, filtered, and concentrated to give a tan solid. Recrystallization from dichloromethane gave 14.18 g (60%) of the title compound as an off-white solid; mp 163-167° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06093744 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-b2525d5950614c7c8d08f494e1e14117 |
| Source note | uspto-grants-2000_07 |