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Water → HCID 22887850, 화합물

HRID 992200
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HRID 992200 반응식
[C:1]([O:8][CH2:9][CH3:10])(=[O:7])[C:2]([O:4]CC)=O.[O:11]1[CH2:15][CH2:14][CH2:13][CH2:12]1.[NH4+].[Cl-].O.[C:19](OCC)(=[O:21])[CH3:20]>>[O:21]1[CH2:19][CH2:20][O:11][CH:15]1[CH2:14][CH2:13][CH2:12][C:2](=[O:4])[C:1]([O:8][CH2:9][CH3:10])=[O:7]
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참가 물질

6

반응물 5

HCID 962WaterHCID 7268Diethyl Oxalate2회HCID 8028TetrahydrofuranHCID 8857Ethyl AcetateHCID 25517Ammonium Chloride

생성물 1

HCID 22887850HCID 22887850, 화합물

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온도
-60 °C

실험 절차

A 1 L 3-necked round bottom flask was equipped with a nitrogen line, overhead stirrer, and thermocouple. Under a nitrogen atmosphere, the flask was charged with diethyl oxalate (73.85 g) and tetrahydrofuran (250 mL). The solution was cooled to −60° C., and the liquid portion of the Grignard reagent was added to the cooled diethyl oxalate solution via cannula to maintain the temperature below −55° C. The Grignard preparation flask was washed with tetrahydrofuran (3×20 mL), and the resulting wash was added via cannula. The addition was complete after 1.5 hours, and the reaction was stirred for about 2 hours at −60° C. to −55° C. The cold reaction mixture was immediately poured into a mixture consisting of NH4Cl (32.1 g), water (100 mL), ice (200 g) and ethyl acetate (300 mL). The layers were separated and the aqueous layer was extracted again with ethyl acetate (2×300 mL). The combined organic layers were dried over magnesium sulfate and concentrated to afford 87 g (79 M % yield) of 5-(1,3-dioxolan-2-yl)-2-oxo-pentanoic acid, ethyl ester as a thick liquid.

후처리

  1. customA 1 L 3-necked round bottom flask was equipped with a nitrogen line, overhead stirrer
  2. temperatureto maintain the temperature below −55° C
  3. customThe Grignard preparation flask
  4. washwas washed with tetrahydrofuran (3×20 mL)
  5. washthe resulting wash
  6. additionwas added via cannula
  7. additionThe addition
  8. customThe cold reaction mixture
  9. additionwas immediately poured into a mixture
  10. customThe layers were separated
  11. extractionthe aqueous layer was extracted again with ethyl acetate (2×300 mL)
  12. dry with materialThe combined organic layers were dried over magnesium sulfate
  13. concentrationconcentrated

출처 및 근거

ORD 기록
ord-3f8084cfc79d4fd0b0ddf81ca055c859
출처 데이터셋
uspto-grants-2002_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06468781B1

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