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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1027907생성일: 2026년 10월 26일

Ethyl diazoacetate → Ethyl 1,3-dimethyl-5-oxo-6,7,8,9-tetrahydro-5H-benzo[7]annulene-6-carboxylate

https://huagongshe.com/reaction/1027907

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl diazoacetateHCID 12192—
반응물3,4-dihydro-5,7-dimethylnaphthalen-1(2H)-oneHCID 83619—
반응물Sodium BicarbonateHCID 516892—
반응물Triethyloxonium tetrafluoroborateHCID 2723982—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물Ethyl 1,3-dimethyl-5-oxo-6,7,8,9-tetrahydro-5H-benzo[7]annulene-6-carboxylateHCID 69225430—

반응 단계

A solution of 5,7-dimethyl-3,4-dihydronaphthalen-1(2H)-one (1 g, 5.74 mmol) in anhydrous CH2Cl2 (20 mL) under nitrogen atmosphere was cooled to 0° C. To this solution was added triethyloxonium tetrafluoroborate (1M in CH2Cl2, 23 mL, 23 mmol), followed with ethyl diazoacetate (1.2 mL, 11.5 mmol). The mixture was stirred at ambient temperature for 16 hrs. The reaction was worked up with saturated sodium bicarbonate, diluted with water and CH2Cl2, and the layers were separated. The organic layer was dried with MgSO4, concentrated and the residue was purified by chromatography on silica gel eluting with 10% EtOAc/Hexanes to provide the title compound. 1H NMR (CD3OD) δ 1.29 (t, 3H), 1.97-2.12 (m, 4H), 2.28-2.30 (m, 3H), 2.30-2.31 (m, 3H), 2.59 (t, 2H), 4.28 (q, 2H), 6.86-6.90 (m, 1H), 6.95-6.99 (m, 1H), 13.17-13.22 (m, 1H). MS (M+H)+ m/z 261.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08735411B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-333643b3f30840b5ad90e20e859667a2
출처 메모uspto-grants-2014_05