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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Diethyl ((3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl)methyl)phosphonate | HCID 70421 | — |
| Catalyst | Pyridine | HCID 1049 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3-Chloro-5-tert. butyl-4-hydroxybenzyl-phosphonic acid diethyl ester | HCID 86735499 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04076690 |
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| Source dataset | uspto-grants-1978_02 |
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| ORD ID | ord-990654cce92842b785073a598741315f |
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| Source note | uspto-grants-1978_02 |
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