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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1283937생성일: 2026년 10월 26일

Sodium hydride → nitro(tetrahydro-2H-1,3-oxazin-2-ylidene)acetic acid

https://huagongshe.com/reaction/1283937

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물2-(Methylthio)ethanolHCID 78925—
반응물Methyl nitro(1,3-oxazinan-2-ylidene)acetateHCID 71444191—
용매DimethylformamideHCID 6228—
생성물nitro(tetrahydro-2H-1,3-oxazin-2-ylidene)acetic acidHCID 73795057—

반응 단계

50 g Of 2-(methylthio)ethanol was added dropwise over a 30-minute period to a stirred mixture of 3.0 g of 57% mineral oil dispersion of sodium hydride in 50 ml of dry dimethylformamide at 0°. The mixture was allowed to warm to room temperature and stirred for 1 hour. Then 6.1 g of 1A was added all at once and the mixture was stirred at room temperature overnight and extracted with ether and with methylene chloride. the aqueous layer was acidified and extracted with methylene chloride. The latter extract was washed with water, dried (MgSO4), decolorized and filtered and the solvent was evaporated under reduced pressure. The residue was crystallized from pentane, then recrystallized from ethyl acetate-ether to give the 2-(methylthio)ethyl ester of nitro(tetrahydro-2H-1,3-oxazin-2-ylidene)acetic acid (1B) as a pale yellow solid, m.p.: 88.5°-89.5°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03976772
출처 데이터셋uspto-grants-1976_08
ORD IDord-905faa1f91e3427e963ee016bfd22847
출처 메모uspto-grants-1976_08