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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Boron trifluoride → 2-Propenoic acid, 2-methyl-, tetrahydro-5-oxo-3-furanyl ester

HRID 526804
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HRID 526804 반응식
[C:1]([O:6][CH2:7][CH:8]1[O:12][C:10](=[O:11])[CH2:9]1)(=[O:5])[C:2]([CH3:4])=[CH2:3].B(F)(F)F>C1(C)C=CC=CC=1>[C:1]([O:6][CH:7]1[CH2:8][O:12][C:10](=[O:11])[CH2:9]1)(=[O:5])[C:2]([CH3:4])=[CH2:3]
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참가 물질

4

반응물 2

HCID 6356Boron trifluorideHCID 57796750beta-Methacryloyloxymethyl-beta-propiolactone

생성물 1

HCID 114010112-Propenoic acid, 2-methyl-, tetrahydro-5-oxo-3-furanyl ester수율 55%

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
30 °C

실험 절차

In a 20 mL Schlenk flask, 2.0 g of crude β-methacryloyloxymethyl-β-propiolactone was put, and dissolved in 8.0 g of toluene. Further, 54 μL of diethyl ether complex of boron trifluoride was added thereto, and the resulting mixture was warmed to 30° C. and stirred. After the mixture was stirred for 2 hours, the resulting reaction mixture was washed with a 10% sodium hydrogen carbonate aqueous solution and saturated brine, and dried over magnesium sulfate. After separation by filtration, the solvent was distilled off using an evaporator to give 1.1 g of crude β-methacryloyloxy-γ-butyrolactone represented by formula (10). FIG. 3 shows an NMR measurement chart.

후처리

  1. stirringAfter the mixture was stirred for 2 hours
  2. customthe resulting reaction mixture
  3. washwas washed with a 10% sodium hydrogen carbonate aqueous solution and saturated brine
  4. dry with materialdried over magnesium sulfate
  5. customAfter separation
  6. filtrationby filtration
  7. distillationthe solvent was distilled off
  8. customan evaporator

출처 및 근거

ORD 기록
ord-64390162edaf468e91ddd3c8a63dff37
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09346775B2

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