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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 76780생성일: 2026년 10월 24일

Dimethylformamide → Methyl 2-(5-tert-butyl-2-hydroxy-4-nitrophenyl)-2-methylpropanoate

https://huagongshe.com/ko/reaction/76780

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Silane, ((1-methoxy-2-methyl-1-propenyl)oxy)trimethyl-HCID 552336—
반응물2-Bromo-4-tert-butyl-5-nitro-phenolHCID 59544145—
촉매Zinc(II) fluorideHCID 10129912—
촉매HCID 178418851HCID 178418851—
용매WaterHCID 962—
생성물Methyl 2-(5-tert-butyl-2-hydroxy-4-nitrophenyl)-2-methylpropanoateHCID 59544161—

반응 조건

온도70 °C

반응 단계

A mixture of 2-bromo-4-tert-butyl-5-nitrophenol (15.00 g, 54.72 mmol), bis(tri-tert-butylphosphine)palladium(0) (1.422 g, 2.783 mmol), zinc fluoride (2.82 g, 27.27 mmol), methyl trimethylsilyl dimethylketene acetal (MTDA) (19.35 g, 111.0 mmol), and dimethylformamide (150 mL) was heated at 70° C. for 18 h. The mixture was cooled to room temperature and diluted with water. After stirring for one hour, the aqueous phase was extracted with MTBE. The organic layer was dried in vacuo to afford the crude product as a brown solid. Purification of the product was accomplished by trituration in n-heptane. 1H-NMR (400 MHZ, DMSO-d6) δ 10.38 (s, 1H); 7.37 (s, 1H); 6.79 (s, 1H); 3.54 (s, 3H); 1.45 (s, 6H); 1.32 (s, 9H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835639B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-b7df57c9d10c4480a2c699a7d163b300
출처 메모uspto-grants-2014_09