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Iodine → HCID 18437784, 화합물

HRID 1375371
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HRID 1375371 반응식
[Li]CCCC.[CH2:6]([N:10]1[CH:14]=[C:13]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[N:12]=[CH:11]1)[CH2:7][CH2:8][CH3:9].[I:21]I.[NH4+].[Cl-]>CCCCCC.C1COCC1>[CH2:6]([N:10]1[CH:14]=[C:13]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[N:12]=[C:11]1[I:21])[CH2:7][CH2:8][CH3:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 807IodineHCID 25517Ammonium ChlorideHCID 184377891-Butyl-4-phenyl-1H-imidazoleHCID 178418339Butyllithium

생성물 1

HCID 18437784HCID 18437784, 화합물

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매2회
HCID 8058
Hexane
용매

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온도
-78 °C

실험 절차

BuLi (1.60 g) in hexane is added to a solution of 1-butyl-4-phenyl-1H-imidazole (4.16 g) in 60 mL of THF. The mixture is stirred at −78° C. for 1 hour. A solution of I2 (5.81 g) in 20 mL of THF is then added dropwise. The resulting mixture is stirred at −78° C. for 30 minutes and then warmed to room temperature. Saturated NH4Cl is added to quench the reaction. The THF is evaporated; the residue is extracted with ethyl acetate, washed with brine, and dried over Na2SO4. Concentration and purification via flash chromatography provides 1-butyl-2-iodo-4-phenyl-1H-imidazole.

후처리

  1. stirringThe resulting mixture is stirred at −78° C. for 30 minutes
  2. temperaturewarmed to room temperature
  3. customto quench
  4. customthe reaction
  5. customThe THF is evaporated
  6. extractionthe residue is extracted with ethyl acetate
  7. washwashed with brine
  8. dry with materialdried over Na2SO4
  9. concentrationConcentration and purification via flash chromatography

출처 및 근거

ORD 기록
ord-0624f87e780e4e0bbd058bc3173cbb6b
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07169775B2

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