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Phosgene → 2-(1-Methoxycarbonylethoxy)benzenesulfonyl isocyanate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Phosgene | HCID 6371 | — |
| 反応物 | Butyl isocyanate | HCID 8110 | — |
| 反応物 | 2-(1-Methoxycarbonylethoxy)benzenesulfonamide | HCID 22152837 | — |
| 触媒 | Diazabicyclooctane | HCID 66583054 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | 2-(1-Methoxycarbonylethoxy)benzenesulfonyl isocyanate | HCID 22152836 | 125.5% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04726836 |
| 出典データセット | uspto-grants-1988_02 |
| ORD ID | ord-256cd9153e88410d975da315b2913afe |
| 出典メモ | uspto-grants-1988_02 |