関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Salicyl Alcohol | HCID 5146 | — |
| 反応物 | Acridine | HCID 9215 | — |
| 反応物 | Thiophosphoryl chloride | HCID 19883 | — |
| 反応物 | Calciumoxide | HCID 6850728 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 2-Chloro-2H,4H-1,3,2lambda~5~-benzodioxaphosphinine-2-thione | HCID 14346679 | — |
反応手順
Into a three-necked, 500 ml flask were placed 31 g (0.25 mole) o-hydroxybenzyl alcohol, 56 g (1.0 moles) calcium oxide, a catalytic amount (0.1 g) of acridine, and 600 ml of benzene. To this reaction mixture was added 46.5 g (0.275 mole) of thiophosphoryl trichloride, dropwise, over a period of 120 minutes with stirring. The temperature was maintained at 22° C by use of a water bath. After the addition of the thiophosphoryl trichloride the mixture was stirred overnight. The mixture was then filtered, the solids washed with four equal portions of benzene (total of 200 ml) and the washings combined with the filtrate. The filtrate was then washed with two equal portions of a 5 percent aqueous bicarbonate solution (total of 100 ml), dried over sodium sulfate, filtered, and the volatiles removed under reduced pressure. The residue crystallized, affording 39 g (71%) pf 2-chloro-4H-1,3,2-benzodioxaphosphorin-2-sulfide, m.p.=44°-45° C. Analysis: %Cl, 16.12 (calculated); 16.42 (Found).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04087490 |
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| 出典データセット | uspto-grants-1978_05 |
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| ORD ID | ord-b9625f5a5c254fd3bba1a0d558b822b0 |
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| 出典メモ | uspto-grants-1978_05 |
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