HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N-Dimethylaniline → 11-Chlorodibenzo(b,f)(1,4)thiazepine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N-Dimethylaniline | HCID 949 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Chlorimide | HCID 76939 | — |
| Reactant | Dibenzothiazepinone | HCID 374829 | — |
| Product | 11-Chlorodibenzo(b,f)(1,4)thiazepine | HCID 10586481 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04879288 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-cc920f4dd6c348c885e92f6e86bf726d |
| Source note | uspto-grants-1989_11 |