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HRID 616814作成日:2026年10月27日

Sulfur Dioxide → 3-Chloro-5-tert. butyl-4-hydroxybenzyl-phosphonic acid diethyl ester

https://huagongshe.com/reaction/616814

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfur DioxideHCID 1119—
反応物Sulfuryl chlorideHCID 24648—
反応物Diethyl ((3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl)methyl)phosphonateHCID 70421—
触媒PyridineHCID 1049—
溶媒Carbon TetrachlorideHCID 5943—
生成物3-Chloro-5-tert. butyl-4-hydroxybenzyl-phosphonic acid diethyl esterHCID 86735499—

反応条件

温度0 °C

反応手順

71.2 g of 3,5-di-tert. butyl-4-hydroxybenzyl-phosphonic acid diethyl ester are dissolved in 200 ml of carbon tetrachloride. After addition of a few drops of pyridine, 40.5 g of sulphuryl chloride are added dropwise, with stirring, at about 0° C in the course of 45 minutes. The reaction mixture is then further stirred for 10 hours at room temperature, in the course of which the formation of sulphur dioxide is observed. After the reaction is terminated, the solvent is removed as far as possible completely in vacuo. The semi-crystalline residue is digested with water and washed neutral and finally recrystallised from aqueous isopropanol in order to purify it. Instead of isopropanol it is also possible to use ethylene glycol monomethyl ether. Toluene is also suitable for effecting recrystallisation, but the crude product must in this case be freed from water beforehand. The 3-chloro-5-tert. butyl-4-hydroxybenzyl-phosphonic acid diethyl ester is obtained in the form of colourless crystals (stabiliser 1) with a melting point of 116° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04076690
出典データセットuspto-grants-1978_02
ORD IDord-990654cce92842b785073a598741315f
出典メモuspto-grants-1978_02