참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 1-Piperidinecarboxaldehyde | HCID 17429 | — |
| 반응물 | 3,7-Dimethoxy-10-methylphenothiazine | HCID 18972534 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Ether tetrahydrofuran | HCID 21868444 | — |
| 생성물 | 3,7-Dimethoxy-10-methyl-phenothiazine-4-carbaldehyde | HCID 18972560 | 179.9% |
반응 단계
16.25 ml of n-butyllithium solution (1.6M in hexane) were added dropwise at -78° under argon to a solution of 5.46 g (10.0 mmol) of 3,7-dimethoxy-10-methylphenothiazine in 100 ml of diethyl ether/tetrahydrofuran (4:1). The reaction mixture was stirred at -70° for 15 minutes, brought slowly to 0°, stirred for 2 hours and then treated at 0° with 3.39 g (30.0 mmol) of N-formylpiperidine. After stirring at 0° for 2 hours the mixture was poured into 500 ml of ice-water, whereupon it was acidified slightly with 0.5N hydrochloric acid solution and extracted with ethyl acetate. The combined organic phases, were extracted with saturated sodium chloride solution, dried over magnesium sulphate and evaporated. The residue was crystallized from acetone, whereupon, after drying, 5.42 g (90%) of 3,7-dimethoxy-10-methyl-phenothiazine-4-carbaldehyde were obtained as a red solid of m.p. 150°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05811389 |
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| 출처 데이터셋 | uspto-grants-1998_09 |
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| ORD ID | ord-b012d55e85ff408dad065163dbbe35fa |
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| 출처 메모 | uspto-grants-1998_09 |
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