HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463383Generated: October 29, 2026
Diisopropyl Ether → Ethyl 2-methoxyimino-3,3-ethylenedioxy-4-chlorobutyrate
https://huagongshe.com/reaction/463383
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Ethyl 2-methoxyimino-3,3-ethylenedioxybutyrate | HCID 54382027 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 2-methoxyimino-3,3-ethylenedioxy-4-chlorobutyrate | HCID 54025463 | — |
Reaction Steps
To a solution of ethyl 2-methoxyimino-3,3-ethylenedioxybutyrate (syn isomer, 30 g) in acetic acid (150 ml) was added lithium chloride (7 g) and the mixture was stirred for 15 minutes at ambient temperature. To the mixture was added dropwise sulfuryl chloride (22.4 g), and the mixture was stirred for one hour at ambient temperature and then allowed to stand for overnight. To the reaction mixture was added water (600 ml) under ice-cooling and stirring, and diisopropyl ether (400 ml) was added thereto and then stirred. The diisopropyl ether layer was separated, and the remaining aqueous layer was further extracted with diisopropyl ether. The diisopropyl ether layer and extract were combined together, washed with water, a saturated aqueous solution of sodium bicarbonate, water and a saturated aqueous solution of sodium chloride in turn, dried over magnesium sulfate and then filtered. The filtrate was concentrated and the residual oil (31.2 g) was distilled under reduced pressure to give ethyl 2-methoxyimino-3,3-ethylenedioxy-4-chlorobutyrate (syn isomer), bp 104°-106° C./0.32-0.35 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04518774 |
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| Source dataset | uspto-grants-1985_05 |
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| ORD ID | ord-320a9666c02b4bb6a92a4b786d6ef09f |
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| Source note | uspto-grants-1985_05 |
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