HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosgene → 2-(1-Methoxycarbonylethoxy)benzenesulfonyl isocyanate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Butyl isocyanate | HCID 8110 | — |
| Reactant | 2-(1-Methoxycarbonylethoxy)benzenesulfonamide | HCID 22152837 | — |
| Catalyst | Diazabicyclooctane | HCID 66583054 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2-(1-Methoxycarbonylethoxy)benzenesulfonyl isocyanate | HCID 22152836 | 125.5% |
Reaction Steps
A mixture of 12.9 g of 2-(1-methoxycarbonylethoxy)-benzenesulfonamide, 4.9 g of n-butylisocyanate and 0.1 g of diazabicyclooctane and 130 ml of xylene is refluxed for 30 minutes. Then 10 g of phosgene are passed into the solution at the same temperature over 90 minutes. Excess phosgene is expelled with nitrogen and the solution is then cooled and concentrated in vacuo, affording 17.7 g of 2-(1-methoxycarbonylethoxy)benzenesulfonyl isocyanate in the form of a brownish oil which can be further used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04726836 |
| Source dataset | uspto-grants-1988_02 |
| ORD ID | ord-256cd9153e88410d975da315b2913afe |
| Source note | uspto-grants-1988_02 |