HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2163428Generated: October 30, 2026
Glycol monoethyl ether → 2-(Chloroethanesulfinyloxy)ethyl 2-chloroethanesulfinate
https://huagongshe.com/reaction/2163428
Participants
| Role | Name | HCID | Charge |
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| Reactant | Glycol monoethyl ether | HCID 8076 | — |
| Reactant | 2-Chloroethanesulfinic chloride | HCID 12550052 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(Chloroethanesulfinyloxy)ethyl 2-chloroethanesulfinate | HCID 54151739 | — |
Reaction Steps
Ethyl glycol (6.2) was added dropwise under a nitrogen atmosphere to a stirred solution of 2-chloroethanesulfinyl chloride (14.7 w), prepared as in Example I, in dry ether (40 v). During the addition period the temperature of the reaction was controlled at -20° by external cooling. Upon completion of the addition, the reaction mixture was warmed to ambient temperature and the solvent was removed by distillation in a vacuum. Examination of the residue by gas-liquid chromatography revealed more than one major component. The residue was then redissolved in dry ether (200 v) and further treated with 2-chloroethanesulfinyl chloride (14.7 w) as above. Using the same procedure as above an oily residue was obtained which after purification in a wiped film molecular still yielded a colorless liquid, 2-(chloroethanesulfinyloxy)ethyl 2-chloroethanesulfinate (8.5 w) boiling at 110-115° under reduced pressure (1 × 10-4 torr).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04134752 |
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| Source dataset | uspto-grants-1979_01 |
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| ORD ID | ord-1ea2fb48474240e0aa750c38425de706 |
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| Source note | uspto-grants-1979_01 |
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