Hydrochloric Acid → 2,3-Piperidinedione 3-(3-bromophenyl)hydrazone
반응식
C([CH:6]1[CH2:11][CH2:10][CH2:9][NH:8][C:7]1=[O:12])(OCC)=O.[OH-].[K+].[Br:15][C:16]1[CH:17]=[C:18]([CH:20]=[CH:21][CH:22]=1)[NH2:19].Cl.[N:24]([O-])=O.[Na+].NC(N)=O.N(O)=O.C(=O)([O-])[O-].[Na+].[Na+]>O>[Br:15][C:16]1[CH:17]=[C:18]([NH:19][N:24]=[C:6]2[CH2:11][CH2:10][CH2:9][NH:8][C:7]2=[O:12])[CH:20]=[CH:21][CH:22]=1참가 물질
반응물 8
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 0 °C
실험 절차
3-Carbethoxy-2-piperidone (4.7 g, 27.4 mmol) is stirred with potassium hydroxide (1.64 g) in water (56 mL) and kept at 30° C. on an oil bath overnight. 3-Bromoaniline (4.99 g, 29 mmol) is treated with water (50 mL) and concentrated HCl (10 mL) and cooled to 0° C. Sodium nitrite (2.46 g, 35 mmol) in water (9 mL) is added dropwise to the above solution at 0° C. and stirred for an additional 20 minutes. Urea is added to decompose the excess nitrous acid, and the diazotized solution is neutralized with 10% aqueous sodium carbonate solution (45-50 mL). The resulting solution is filtered into the solution of previously hydrolyzed 3-carbethoxy-2-piperidone (2-piperidone-3-carboxylic acid) at 0° C. After a few minutes, glacial acetic acid is added to bring the pH of the solution to 3-4. The reaction mixture is stirred at 0° C. for 5-6 h, and the yellow precipitate which resulted is filtered, washed with water, and dried to get the title compound (2.5 g, 32% yield).
후처리
- filtrationThe resulting solution is filtered into the solution of previously hydrolyzed 3-carbethoxy-2-piperidone (2-piperidone-3-carboxylic acid) at 0° C
- waitAfter a few minutes
- additionglacial acetic acid is added
- stirringThe reaction mixture is stirred at 0° C. for 5-6 h
- customthe yellow precipitate which resulted
- filtrationis filtered
- washwashed with water
- customdried
출처 및 근거
- ORD 기록
- ord-d86f98e4c494478abb1ff99de2570e51
- 출처 데이터셋
- uspto-grants-2013_01
- 특허 번호
- US08362063B2
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