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Nitromethane → (1-Nitromethyl-cyclobutyl)-acetic Acid Ethyl Ester

HRID 897170
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반응식

HRID 897170 반응식
[CH2:1]([O:3][C:4](=[O:10])[CH:5]=[C:6]1[CH2:9][CH2:8][CH2:7]1)[CH3:2].[N+:11]([CH3:14])([O-:13])=[O:12].[F-].C([N+](CCCC)(CCCC)CCCC)CCC>O1CCCC1.C(OCC)(=O)C>[CH2:1]([O:3][C:4](=[O:10])[CH2:5][C:6]1([CH2:14][N+:11]([O-:13])=[O:12])[CH2:9][CH2:8][CH2:7]1)[CH3:2]
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참가 물질

6

반응물 3

HCID 6375NitromethaneHCID 2724141Tetrabutylammonium FluorideHCID 15724666Cyclobutylidene-acetic acid ethyl ester

생성물 1

HCID 54347145(1-Nitromethyl-cyclobutyl)-acetic Acid Ethyl Ester수율 52.1%

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 8857
Ethyl Acetate
용매

실험 절차

The unsaturated ester (2) (5.79 g, 41.4 mmol) was dissolved in tetrahydrofuran (20 mL) and stirred at 70° C. with nitromethane (4.67 mL, 86.4 mmol) and tetrabutylammonium fluoride (1.0 M in tetrahydrofuran, 55 mL, 55.0 mmol). After 18 hours, the mixture was cooled to room temperature, diluted with ethyl acetate (150 mL), and washed with 2N HCl (60 mL) followed by brine (100 mL). The organic phase was collected, dried (MgSO4), and the solvent removed in vacuo. The residue was purified by flash chromatography (silica, ethyl acetate:heptane 1:1) to give 4.34 g (52%) of a clear oil.

후처리

  1. washwashed with 2N HCl (60 mL)
  2. customThe organic phase was collected
  3. dry with materialdried (MgSO4)
  4. customthe solvent removed in vacuo
  5. customThe residue was purified by flash chromatography (silica, ethyl acetate:heptane 1:1)

출처 및 근거

ORD 기록
ord-df629faf40af426fab363e568fffe13a
출처 데이터셋
uspto-grants-2005_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06921835B2

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