참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-Formylmorpholine | HCID 20417 | — |
| 반응물 | 2-(4-Bromophenyl)-1,3-dioxolane | HCID 2773842 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-(1,3-Dioxolan-2-yl)benzaldehyde | HCID 11829988 | 101.3% |
반응 단계
To a tetrahydrofuran (100 mL) solution of 2-(4-bromo-phenyl)-1,3-dioxolane (8 g, 34.9 mmol) was added dropwise n-butyl lithium (19.6 mL, 2.67 M hexane solution, 52.4 mmol) at −78° C. After 1 hour of stirring at −78° C., N-formylmorpholine (4.42 g, 38.4 mmol) was added to the mixture, and stirred for 3 hours at the same temperature. This mixture was partitioned into diethyl ether and water. The organic layer was separated, washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure to obtain the title compound (6.3 g). This compound was used in the subsequent reaction without being purified.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08841327B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-ebf8b95b75e946869214714f5fd69448 |
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| 출처 메모 | uspto-grants-2014_09 |
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