Cyclohexanone Oxime → Benzyl 2-oxa-3-azabicyclo[2.2.1]hept-5-ene-3-carboxylate
반응식
[C:1]1(=[N:7][OH:8])[CH2:6][CH2:5][CH2:4][CH2:3]C1.ClCl.C([O-])([O-])=O.[Na+].[Na+].Cl[C:18]([O:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)=[O:19].C1CC=CC=1>O.C(OC)(C)(C)C>[CH:4]12[CH2:3][CH:1]([CH:6]=[CH:5]1)[N:7]([C:18]([O:20][CH2:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)=[O:19])[O:8]2참가 물질
반응 조건
- 온도
- -10 °C
실험 절차
Cyclohexanone oxime (20.04 g, 171.8 mmol) and methyl t-butyl ether (110 mL) were added to a reactor at 25° C. and stirred under N2 (g). The solution was cooled to −10° C. and Cl2 (g) was added during 15 min until a deep blue, clear solution was obtained. Vacuum was applied to remove remaining Cl2 and possible HCl from the reaction mixture. The temperature was set to −2° C., and a solution of Na2CO3 (11.03 g, 103 mmol) in water (90 mL) was slowly added during 30 min. The phases were separated and the organic phase transferred to a solution of Na2CO3 (19.3 g, 180.3 mmol) in water (126 mL) at 15° C. Benzyl chloroformate (32.3 g, 179.87 mmol) was added and the reaction mixture stirred for 10 min after which cyclopentadiene (25.2 g, 362.16 mmol) was added and the reaction mixture stirred for 3 h. Vacuum was applied and the remaining cyclopentadiene was removed. The phases were separated and the organic phase containing the title product was taken further directly to Example 2 as below.
후처리
- customwas obtained
- customto remove
- customwas set to −2° C.
- customThe phases were separated
- additionwas added
- stirringthe reaction mixture stirred for 3 h
- customthe remaining cyclopentadiene was removed
- customThe phases were separated
- additionthe organic phase containing the title product
출처 및 근거
- ORD 기록
- ord-5577c84a0d6e4961a8d6789555c6aa31
- 출처 데이터셋
- uspto-grants-2015_07
- 특허 번호
- US09079873B2
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