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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351799Generated: October 30, 2026

Hydrochloric Acid → HCID 12993971, compound

https://huagongshe.com/reaction/351799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 12993970HCID 12993970—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12993971HCID 1299397152.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743814B2
Source datasetuspto-grants-2004_06
ORD IDord-4433565374f54faeb9a53d2762197b27
Source noteuspto-grants-2004_06