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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1853948생성일: 2026년 10월 27일

Cesium carbonate → 3-(1,4-Dioxa-8-aza-spiro[4.5]dec-8-yl)-4-methyl-benzoic acid methyl ester

https://huagongshe.com/reaction/1853948

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
반응물Methyl 3-bromo-4-methylbenzoateHCID 7015747—
용매TolueneHCID 1140—
생성물3-(1,4-Dioxa-8-aza-spiro[4.5]dec-8-yl)-4-methyl-benzoic acid methyl esterHCID 67354675—

반응 단계

A mixture of 2,2′-Bis(diphenylphosphino)1,1′-binaphthyl[BINAP] (54.35 mg, 0.085 mmol) and Palladium(II)acetate[Pd(OAc)2] (6.95 mg, 0.028 mmol) in dry toluene (3 ml) was stirred vigorously and nitrogen was bubbled through the suspension for 30 minutes. To this, 1,4-Dioxa-8-aza-spiro[4.5]-decane (100 mg, 0.699 mmol), 3-Bromo-4-methyl-benzoic acid methyl ester (192.1 mg, 0.839 mmol) and dry Cesium Carbonate (683.5 mg, 2.09 mmol) was added. Nitrogen was bubbled through for another 30 minutes; the mixture was allowed to reflux overnight. The mixture was cooled, diluted with ethylacetate, water was added and the layers separated. The aqueous layer was extracted with ethyl acetate) and the two organic extracts were combined. The organics were washed with brine, then dried (sodium sulfate), filtered and concentrated. Further purification by silica gel chromatography using 5-10% ethyl acetate/Hexane as eluent provided 3-(1,4-Dioxa-8-aza-spiro[4.5]dec-8-yl)-4-methyl-benzoic acid methyl ester [11] as a yellow solid [150.5 mg, 61.7%]

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08962637B2
출처 데이터셋uspto-grants-2015_02
ORD IDord-f2e0da60e2dd48eeaa25344f32643f4a
출처 메모uspto-grants-2015_02