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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616814Generated: October 25, 2026

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

https://huagongshe.com/reaction/616814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfur DioxideHCID 1119—
ReactantSulfuryl chlorideHCID 24648—
ReactantDiethyl ((3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl)methyl)phosphonateHCID 70421—
CatalystPyridineHCID 1049—
SolventCarbon TetrachlorideHCID 5943—
Product3-Chloro-5-tert. butyl-4-hydroxybenzyl-phosphonic acid diethyl esterHCID 86735499—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04076690
Source datasetuspto-grants-1978_02
ORD IDord-990654cce92842b785073a598741315f
Source noteuspto-grants-1978_02