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Diethyl Ether → HCID 58787323, 화합물

HRID 1375651
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HRID 1375651 반응식
[I:1][C:2]1[CH:3]=[C:4](/[CH:8]=[CH:9]/[C:10](OCC)=[O:11])[CH:5]=[CH:6][CH:7]=1.CC(C[AlH]CC(C)C)C.C(C(C(C([O-])=O)O)O)([O-])=O.[K+].[Na+].C(OCC)C>C1COCC1>[I:1][C:2]1[CH:3]=[C:4](/[CH:8]=[CH:9]/[CH2:10][OH:11])[CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 3283Diethyl EtherHCID 14487Diisobutylaluminum hydrideHCID 9855836Potassium sodium tartarateHCID 15508352ethyl (2E)-3-(3-iodophenyl)acrylate

생성물 1

HCID 58787323HCID 58787323, 화합물수율 94%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran
용매

실험 절차

The material from Example 1A (2.0 mmol) was dissolved in THF (10 mL). DIBAL-H (1 M in hexane, 6 mL, 6.0 mmol) was added. The reaction mixture was stirred at ambient temperature for 30 minutes. Saturated sodium potassium tartrate solution was added slowly at 0° C., followed by addition of diethyl ether. The mixture was stirred vigorously overnight. The organic phase was separated and washed with brine, dried (MgSO4), filtered and concentrated under reduced pressure to provide titled compound (489 mg). MS (ESI(−)) m/e 259 (M−H)+; 1H NMR (300 MHz, DMSO-d6) δ 7.79(t, J=1.7 Hz, 1H), 7.57 (dt, J1=1.7 Hz, J2=7.8 Hz, 1H), 7.45 (dt, J1=1.7 Hz, J2=7.8 Hz, 1H), 7.12 (t, J=7.8 Hz, 1H), 6.48–6.42 (m, 2H), 4.89 (t, J=5.8 Hz, 1H), 4.11 (m, 2H).

후처리

  1. stirringThe mixture was stirred vigorously overnight
  2. customThe organic phase was separated
  3. washwashed with brine
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-07b3433364744b4185e46383b6452ca1
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07169797B2

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