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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351797Generated: October 25, 2026

Ammonium Chloride → 5-Methoxymethyl-2-(3,4,4-trifluoro-3-butenylthio)oxazole

https://huagongshe.com/reaction/351797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantBromomethyl methyl etherHCID 83093—
Reactant2-(3,4,4-Trifluoro-3-butenylthio)oxazoleHCID 12993958—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product5-Methoxymethyl-2-(3,4,4-trifluoro-3-butenylthio)oxazoleHCID 2271464313.2%

Reaction Steps

10.40 ml of n-butyl lithium (1.6 M n-hexane solution) were slowly added dropwise to a solution of 3.14 g of 2-(3,4,4-trifluoro-3-butenylthio)oxazole in 40 ml of ether at −70° C. After stirring for 1 hour, a solution of 2.06 g bromomethyl methyl ether in 10 ml ether was added dropwise. After bringing the mixture back to room temperature and stirring for 1 hour, 50 ml of saturated solution of ammonium chloride was added to separate it into an ether layer and an aqueous layer. The aqueous layer was further extracted with ether and together with the separated ether layer it was washed with a saturated sodium chloride water and dried with anhydrous magnesium sulfate. After the solvent was distilled off under reduced pressure, the residue was treated by column chromatography to obtain 0.5 g of 5-methoxymethyl-2-(3,4,4-trifluoro-3-butenylthio)oxazole (yield 13%). n20D=1.4705.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743814B2
Source datasetuspto-grants-2004_06
ORD IDord-5c93f45f4f014b839b8462967fe84277
Source noteuspto-grants-2004_06