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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 351797생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/351797

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물Bromomethyl methyl etherHCID 83093—
반응물2-(3,4,4-Trifluoro-3-butenylthio)oxazoleHCID 12993958—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
생성물5-Methoxymethyl-2-(3,4,4-trifluoro-3-butenylthio)oxazoleHCID 2271464313.2%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06743814B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-5c93f45f4f014b839b8462967fe84277
출처 메모uspto-grants-2004_06