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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 490992생성일: 2026년 10월 23일

N-Methoxy-N-methylacetamide → 1-(2,2-Dimethyl-2,4-dihydro-1,3-benzodioxin-6-yl)ethan-1-one

https://huagongshe.com/ko/reaction/490992

반응식

참여 물질

역할이름HCID투입량
반응물N-Methoxy-N-methylacetamideHCID 537505—
반응물6-Bromo-2,2-dimethyl-4H-benzo[d][1,3]dioxineHCID 14520338—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물1-(2,2-Dimethyl-2,4-dihydro-1,3-benzodioxin-6-yl)ethan-1-oneHCID 21880610—

반응 단계

To the product of step (a) (110 g, 0.46 mol) in 1.0 L of THF at −78° C. was added 236 mL (0.51 mol) of 2.14 M n-butyllithium in hexanes via a dropping funnel. After 30 minutes, N-methyl-N-methoxy acetamide (71 g, 0.69 mol, available from TCI) was added. After 2 hours, the reaction mixture was quenched with water, diluted with 2.0 L of 1.0 M aqueous phosphate buffer (pH=7.0) and extracted once with diethyl ether. The diethyl ether phase was washed once with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to give a light orange oil. The oil was dissolved in a minimum volume of ethyl acetate, diluted with hexanes, and to give the title compound as a crystalline solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07528253B2
출처 데이터셋uspto-grants-2009_05
ORD IDord-4a2edf8a96af45adb0600e1fa74cbeb1
출처 메모uspto-grants-2009_05