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HRID 1027907作成日:2026年10月27日

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

https://huagongshe.com/reaction/1027907

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl diazoacetateHCID 12192—
反応物3,4-dihydro-5,7-dimethylnaphthalen-1(2H)-oneHCID 83619—
反応物Sodium BicarbonateHCID 516892—
反応物Triethyloxonium tetrafluoroborateHCID 2723982—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物Ethyl 1,3-dimethyl-5-oxo-6,7,8,9-tetrahydro-5H-benzo[7]annulene-6-carboxylateHCID 69225430—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08735411B2
出典データセットuspto-grants-2014_05
ORD IDord-333643b3f30840b5ad90e20e859667a2
出典メモuspto-grants-2014_05