Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1966159생성일: 2026년 10월 25일
Diethyl (cyanomethyl)phosphonate → Diisopropyl 3-(cyanomethylene)cyclobutane-1,1-dicarboxylate
https://huagongshe.com/reaction/1966159
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Diethyl (cyanomethyl)phosphonate | HCID 75676 | — |
| 반응물 | 1,1-Bis(propan-2-yl) 3-oxocyclobutane-1,1-dicarboxylate | HCID 4913357 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Diisopropyl 3-(cyanomethylene)cyclobutane-1,1-dicarboxylate | HCID 66823993 | 90.8% |
반응 단계
To a mixture of 1.0000 M of potassium tert-butoxide in tetrahydrofuran (17 mL) and THF (10 mL) was added dropwise, at 0° C., diethyl cyanomethylphosphonate (2.7 mL, 0.017 mol). The reaction was warmed to rt and 30 min later cooled to 0° C. again. To the reaction mixture was added a solution of diisopropyl 3-oxocyclobutane-1,1-dicarboxylate (2.7 g, 0.011 mol) in THF (10 mL). The reaction was allowed to warm up to rt gradually and stirred at rt for 2 h. The reaction was quenched with saturated aq. NH4Cl and the organic solvent was reduced. The mixture was extracted with EtOAc. The combined organic layers were washed with brine, dried over MgSO4, concentrated and purified with Combiflash (silica gel, 0-35% EtOAc/Hex) to give the desired product (2.65 g) as light yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08420629B2 |
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| 출처 데이터셋 | uspto-grants-2013_04 |
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| ORD ID | ord-bdfe24814a8b481bbee138337cd49553 |
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| 출처 메모 | uspto-grants-2013_04 |
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