HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351799Generated: October 30, 2026
Hydrochloric Acid → HCID 12993971, compound
https://huagongshe.com/reaction/351799
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 12993970 | HCID 12993970 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12993971 | HCID 12993971 | 52.5% |
Reaction Steps
A solution of 2.7 g of 4-hydroxymethyl-2-(3,4,4-trifluoro-3-butenylthio)oxazole in 50 ml of tetrahydrofuran (dehydrated) was added dropwise to a suspension of 0.5 g NaH (purity about 60%) in 20 ml of tetrahydrofuran (dehydrated) at 0° C. After stirring the mixture at room temperature for 1 hour, a solution of 2.0 g of methyl iodide in 20 ml of tetrahydrofuran (dehydrated) was added at 0° C. and further stirred at room temperature for 1 hour. The reaction mixture was poured into a mixed solution of 200 g ice and 2N hydrochloric acid. After extraction with 100 ml of dichloromethane, the solution was washed with water and dried with anhydrous magnesium sulfate. After the solvent was distilled off under reduced pressure, the residue was purified by column chromatography (eluent: dichloromethane) to obtain 1.5 g of 4-methoxymethyl-2-(3,4,4-trifluoro-3-butenylthio)oxazole as colorless oil (yield 52.5%). n20D=1.4710.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06743814B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-4433565374f54faeb9a53d2762197b27 |
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| Source note | uspto-grants-2004_06 |
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