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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl diazoacetate | HCID 12192 | — |
| 반응물 | 3,4-dihydro-5,7-dimethylnaphthalen-1(2H)-one | HCID 83619 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Triethyloxonium tetrafluoroborate | HCID 2723982 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Ethyl 1,3-dimethyl-5-oxo-6,7,8,9-tetrahydro-5H-benzo[7]annulene-6-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08735411B2 |
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| 출처 데이터셋 | uspto-grants-2014_05 |
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| ORD ID | ord-333643b3f30840b5ad90e20e859667a2 |
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| 출처 메모 | uspto-grants-2014_05 |
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