戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 371694作成日:2026年10月26日

Salicyl Alcohol → 2-Chloro-2H,4H-1,3,2lambda~5~-benzodioxaphosphinine-2-thione

https://huagongshe.com/reaction/371694

反応式

関与物質

役割名称HCID仕込み量
反応物Salicyl AlcoholHCID 5146—
反応物AcridineHCID 9215—
反応物Thiophosphoryl chlorideHCID 19883—
反応物CalciumoxideHCID 6850728—
溶媒BenzeneHCID 241—
生成物2-Chloro-2H,4H-1,3,2lambda~5~-benzodioxaphosphinine-2-thioneHCID 14346679—

反応条件

温度22 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04087490
出典データセットuspto-grants-1978_05
ORD IDord-b9625f5a5c254fd3bba1a0d558b822b0
出典メモuspto-grants-1978_05