Ethyl diazoacetate → HCID 53959852, 화합물
반응식
[Cl:1][C:2]1[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][C:3]=1[C:9](Cl)=[O:10].[N+:12](=[CH:14][C:15]([O:17][CH2:18][CH3:19])=[O:16])=[N-:13].CC1(C)CCCC(C)(C)N1.[Li]>C1COCC1>[CH2:18]([O:17][C:15](=[O:16])[C:14](=[N+:12]=[N-:13])[C:9]([C:3]1[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][C:2]=1[Cl:1])=[O:10])[CH3:19]참가 물질
실험 절차
To a solution of 2-chlorocyclohept-1-enecarbonyl chloride (4.6 g) and ethyl diazoacetate (2.8 ml) in THF (30 ml) cooled to −70C was added a solution of lithium 2,2,6,6-tetramethylpiperidine (1 equiv.) dropwise. On completion of the addition the reaction mixture was stirred for 1 h. The reaction mixture was quenched by pouring into 1M citric acid (100 ml), then extracted with ether (3×200 ml). The ether extracts were combined, washed with brine, dried over magnesium sulphate, filtered and evaporated under reduced pressure to give an oil. The oil was purified by flash chromatography using a gradient elution: hexane/ether (10:1) 500 ml, hexane/ether (9:1) 500 ml, hexane/ether (8:2) 500 ml. The appropriate fractions were combined and evaporated under reduced pressure to give a yellow oil. δH (360 MHz; CDCl3) 1.33 (3H, t, J=7 Hz, CH3), 1.74 (6H, m, CH2), 2.32 (2H, m, CH2), 2.64 (2H, m, CH2), 4.29 (2H, t, J=7 Hz, CH2).
후처리
- additionOn completion of the addition the reaction mixture
- customThe reaction mixture was quenched
- additionby pouring into 1M citric acid (100 ml)
- extractionextracted with ether (3×200 ml)
- washwashed with brine
- dry with materialdried over magnesium sulphate
- filtrationfiltered
- customevaporated under reduced pressure
- customto give an oil
- customThe oil was purified by flash chromatography
- washa gradient elution
- customevaporated under reduced pressure
- customto give a yellow oil
출처 및 근거
- ORD 기록
- ord-63255e2c5df9476b931ca259708c0104
- 출처 데이터셋
- uspto-grants-2001_01
- 특허 번호
- US06180630B2
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