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Hydrochloric Acid → Ethyl 2,3-dihydro-3-oxo-1H-pyrazole-4-carboxylate

HRID 1697459
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HRID 1697459 반응식
[O-]CC.[Na+].C([O:7][CH:8]=[C:9]([C:15](OCC)=O)[C:10]([O:12][CH2:13][CH3:14])=[O:11])C.O.[NH2:21][NH2:22].Cl>C(O)C.O>[CH2:13]([O:12][C:10]([C:9]1[C:8](=[O:7])[NH:21][NH:22][CH:15]=1)=[O:11])[CH3:14]
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참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 6871Diethyl (ethoxymethylene)malonateHCID 24654Hydrazine hydrate (1:1)HCID 2723922Sodium ethoxide

생성물 1

HCID 238933Ethyl 2,3-dihydro-3-oxo-1H-pyrazole-4-carboxylate수율 84.5%

시약·촉매·용매 2

HCID 702Ethanol용매
HCID 962Water용매

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온도
80 °C

실험 절차

To a solution of sodium ethoxide (20.8 g, 0.31 mol) and diethyl ethoxymethylenemalonate (20 mL, 0.10 mol) in ethanol (400 mL), was added hydrazine monohydrate (10.0 mL, 0.20 mol) with cooling in an ice-cold water bath. The mixture was then heated at 80° C. for 3 h. The resulting mixture was diluted with water (200 mL) and neutralized with 10M HCl solution until pH 6. The mixture was extracted several times with chloroform. The aqueous layer was acidified to pH 2 and extracted again with chloroform. The combined organic layers were dried (Na2SO4) and concentrated to a solid which was washed with methanol and ether and dried to give the product (13.2 g, 80%) as a solid. 1H NMR (400 MHz, DMSO-d6) δ7.89 (s, 1H), 4.15 (q, 211, J=7.12 Hz), 1.23 (t, 3H, J=7.11 Hz).

후처리

  1. temperaturewith cooling in an ice-cold water bath
  2. extractionThe mixture was extracted several times with chloroform
  3. extractionextracted again with chloroform
  4. dry with materialThe combined organic layers were dried (Na2SO4)
  5. concentrationconcentrated to a solid which
  6. washwas washed with methanol and ether
  7. customdried

출처 및 근거

ORD 기록
ord-9c6aeca92955443a8f250568a8ec23b4
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08163901B2

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