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Methanol → Methyl[1-(3-bromopropyl)cyclopropyl]acetate

HRID 238166
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HRID 238166 반응식
[CH2:1]([C:4]1([CH2:7][C:8]([O:10][CH3:11])=[O:9])[CH2:6][CH2:5]1)[CH:2]=[CH2:3].CO.[Br:14]Br.C[O-].[Na+].C(=O)(O)[O-].[Na+]>C1COCC1>[CH3:11][O:10][C:8](=[O:9])[CH2:7][C:4]1([CH2:1][CH2:2][CH2:3][Br:14])[CH2:5][CH2:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 887MethanolHCID 24408BromineHCID 516892Sodium BicarbonateHCID 10942334Sodium MethoxideHCID 58074534Methyl[1-(prop-2-en-1-yl)cyclopropyl]acetate

생성물 1

HCID 58074516Methyl[1-(3-bromopropyl)cyclopropyl]acetate

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매
2회

실험 절차

Under argon and at 0° C., 3.4 ml (3.4 mmol) of borane/THF complex solution (1 M in THF) were added dropwise to 1542 mg (10 mmol) of methyl [1-(prop-2-en-1-yl)cyclopropyl]acetate in 10 ml of anhydrous THF. After 30 min at 0° C., the reaction was stirred at RT for a further 30 min, and 22 μl (0.54 mmol) of methanol were then added. At −5° C., 0.62 ml (12 mmol) of bromine and 2971 mg (16.5 mmol) of sodium methoxide solution (30% in methanol) were then successively added dropwise to the reaction mixture. Once the reaction had reached room temperature, 10 ml of saturated sodium bicarbonate solution were added, the organic phase was separated off and the aqueous phase was extracted three more times with tert-butyl methyl ether. The combined organic phases were washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. Removal of the solvent under reduced pressure gave 683 mg (2.9 mmol, 29% of theory) of the title compound as a yellow oil.

후처리

  1. customhad reached room temperature
  2. customthe organic phase was separated off
  3. extractionthe aqueous phase was extracted three more times with tert-butyl methyl ether
  4. washThe combined organic phases were washed with saturated sodium chloride solution
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customRemoval of the solvent under reduced pressure

출처 및 근거

ORD 기록
ord-58bcb16fdd444a31898f12fffc5e1290
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08642592B2

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