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N,N-Dimethylaniline → 11-Chlorodibenzo(b,f)(1,4)thiazepine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N,N-Dimethylaniline | HCID 949 | — |
| 反応物 | Phosphorus oxychloride | HCID 24813 | — |
| 反応物 | Chlorimide | HCID 76939 | — |
| 反応物 | Dibenzothiazepinone | HCID 374829 | — |
| 生成物 | 11-Chlorodibenzo(b,f)(1,4)thiazepine | HCID 10586481 | — |
反応手順
A 2 liter round-bottom flask equipped with a magnetic stirring bar and reflux condenser with a nitrogen inlet was charged with 115.0 g (0.506 mole) of dibenzo[b,f][1,4]thiazepine-11(10-H)one, phosphorous oxychloride 700 ml (7.5 moles) and N,N-dimethylaniline 38.0 g (0.313 mole). The grey suspension was heated to gentle refluxing using a heating mantle. After 6 hours of heating, the resulting amber solution was allowed to cool to room temperature (from about 18°-25°C.) and was analyzed by thin-layer chromatography (TLC) using silica gel plates, developed with ether-hexane (1:1) and detected with ultraviolet light. Analysis revealed the desired imino chloride, Rf =0.70, and an absence of starting lactam.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04879288 |
| 出典データセット | uspto-grants-1989_11 |
| ORD ID | ord-cc920f4dd6c348c885e92f6e86bf726d |
| 出典メモ | uspto-grants-1989_11 |