HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822639Generated: October 29, 2026
Chloromethyl ethyl ether → HCID 54413931, compound
https://huagongshe.com/reaction/1822639
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloromethyl ethyl ether | HCID 18523 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 57031928 | HCID 57031928 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54413931 | HCID 54413931 | 14.4% |
Reaction Steps
0.6 g of 2-{2-tert-butyloxazol-4-yl}-3-(5-chloro-3-trifluoromethyl-1-methyl-pyrazol-4-yl)-3-hydroxyacrylonitrile was dissolved in 5 ml of THF, and 0.07 g of 60% sodium hydride was added thereto with cooling with ice, and then stirred for 15 minutes at room temperature. 0.17 g of ethoxymethyl chloride was added thereto and stirred for 6 days at room temperature. The reaction mixture was poured into ice water, extracted with ethyl acetate, and washed with saturated saline. The resulting product was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The resulting residual product was purified through silica gel thin-layer chromatography (ethyl acetate:n-hexane=1:4) to obtain 0.1 g of the intended compound in vitreous state.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07037880B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-21a0d51a88e948c9b0a3f37dc1c9bec9 |
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| Source note | uspto-grants-2006_05 |
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