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Hydrochloric Acid → (+/-)-4-(Prop-2-en-1-yloxy)pent-1-en-3-one

HRID 242019
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HRID 242019 반응식
CON(C)[C:4](=[O:11])[CH:5]([O:7][CH2:8][CH:9]=[CH2:10])[CH3:6].[CH:13]([Mg]Br)=[CH2:14].Cl>O1CCCC1>[CH2:8]([O:7][CH:5]([CH3:6])[C:4](=[O:11])[CH:13]=[CH2:14])[CH:9]=[CH2:10]
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참가 물질

5

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HCID 313Hydrochloric AcidHCID 86660003(+/-)-N-Methoxy-N-methyl-2-(prop-2-en-1-yloxy)propanamideHCID 178418507HCID 178418507, 화합물

생성물 1

HCID 86660004(+/-)-4-(Prop-2-en-1-yloxy)pent-1-en-3-one

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
-78 °C

실험 절차

(±)-N-Methoxy-N-methyl-2-(prop-2-en-1-yloxy)propanamide (1.26 g, 7.27 mmol) was dissolved in tetrahydrofuran (20 mL) and cooled to −78° C. Vinylmagnesium bromide (11.4 mL, 0.7 M solution in tetrahydrofuran, 8.00 mmol, 1.1 equiv) was added and the mixture was stirred at −78° C. for 10 minutes. Hydrochloric acid (5 mL, 4 M aqueous) was added, the mixture was warmed to ambient temperature and extracted with chloroform (2×30 mL). The combined organic extracts were dried with sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by silica gel gradient chromatography (100:0 to 30:70; hexanes:ethyl acetate), providing the titled compound.

후처리

  1. temperaturethe mixture was warmed to ambient temperature
  2. extractionextracted with chloroform (2×30 mL)
  3. dry with materialThe combined organic extracts were dried with sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by silica gel gradient chromatography (100:0 to 30:70; hexanes:ethyl acetate)

출처 및 근거

ORD 기록
ord-e2119f75af6f47bd943605c48b41b578
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08653079B2

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