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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 19005115, 화합물 → HCID 19005118, 화합물

HRID 2225918
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HRID 2225918 반응식
O=C1[CH:6]([C:7](=[O:17])[C:8]([F:16])([F:15])[CH2:9][CH2:10][C:11]([CH3:14])([CH3:13])[CH3:12])[CH2:5][CH2:4][O:3]1>Cl.C(O)(=O)C>[OH:3][CH2:4][CH2:5][CH2:6][C:7](=[O:17])[C:8]([F:16])([F:15])[CH2:9][CH2:10][C:11]([CH3:12])([CH3:13])[CH3:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 19005115HCID 19005115, 화합물

생성물 1

HCID 19005118HCID 19005118, 화합물

시약·촉매·용매 2

HCID 313Hydrochloric Acid촉매HCID 176Acetic Acid용매

실험 절차

A 10 mL one neck round bottom flask, fitted with argon inlet, magnetic stirrer, and reflux condenser was charged with 1.0 mL glacial acetic acid, 4 drops of concentrated HCl and 200 mg(0.81 mM) of 2,3,4,5-tetrahydro-2-oxo-3-(5,5-dimethyl-2,2-difluoro-1-oxohexyl)furan. The reaction mixture was heated at 110 C. overnight under a blanket of argon. The reaction was extracted with ethyl ether, and the ether was cross washed with water, dried (anhydrous MgSO4), and solvent removed under reduced pressure. The residue was chromatographed on a 10×60 mm silica gel column using a 9:1 hexane:ethyl acetate mixture to give a clear oil. nmr(CDCl3) -L 0.95(s,9H), 1.45(t,2H), 2.00(m,6H), 3.12(bs,1H), 4.15(m,1H)

후처리

  1. temperaturereflux condenser
  2. temperatureThe reaction mixture was heated at 110 C
  3. customovernight
  4. extractionThe reaction was extracted with ethyl ether
  5. washthe ether was cross washed with water
  6. dry with materialdried (anhydrous MgSO4), and solvent
  7. customremoved under reduced pressure
  8. customThe residue was chromatographed on a 10×60 mm silica gel column
  9. customethyl acetate mixture to give a clear oil

출처 및 근거

ORD 기록
ord-7d17f65273b54cba80e4a3ed0a29fb24
출처 데이터셋
uspto-grants-1994_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05344952

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