Sodium Iodide → HCID 49765294, 화합물

HRID 537671노트

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HRID 537671 반응식
Br[C:2]1[CH:3]=[CH:4][C:5]([CH2:16][CH3:17])=[C:6]([CH:8]2[C:13](=[O:14])[CH2:12][CH2:11][CH2:10][C:9]2=[O:15])[CH:7]=1.[I-:18].[Na+].C[Si](C)(C)N[Si](C)(C)C.CN(C)[C@@H]1CCCC[C@H]1N>[Cu]I.O1CCOCC1>[CH2:16]([C:5]1[CH:4]=[CH:3][C:2]([I:18])=[CH:7][C:6]=1[CH:8]1[C:13](=[O:14])[CH2:12][CH2:11][CH2:10][C:9]1=[O:15])[CH3:17]

참가 물질

7

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온도
180 °C

실험 절차

To a mixture of 2-(5-bromo-2-ethylphenyl)cyclohexane-1,3-dione (0.917 g, 3.11 mmol), sodium iodide (0.934 g, 6.23 mmol) and hexamethyldisilazane (0.454 g, 3.11 mmol) is added copper (I) iodide (0.030 g, 0.15 mmol) and trans-N,N-dimethyl-1,2-cyclohexane diamine (0.044 g, 0.31 mmol). Degassed dioxane (5 ml) is added and the mixture is purged with nitrogen then heated at 180° C. for 1 hour under microwave irradiation. After cooling to room temperature the reaction mixture is treated with 2M aqueous hydrochloric acid and extracted with dichloromethane. The phases are separated and the aqueous phase is further extracted with dichloromethane. Organic fractions are combined then evaporated under reduced pressure to yield a crude product which is purified by flash column chromatography (10% ethyl acetate/hexane to 70% ethyl acetate/hexane eluant) to afford 2-(2-ethyl-5-iodophenyl)cyclohexane-1,3-dione as a white foam.

후처리

  1. customthe mixture is purged with nitrogen
  2. temperatureAfter cooling to room temperature the reaction mixture
  3. additionis treated with 2M aqueous hydrochloric acid
  4. extractionextracted with dichloromethane
  5. customThe phases are separated
  6. extractionthe aqueous phase is further extracted with dichloromethane
  7. customOrganic fractions are combined then evaporated under reduced pressure
  8. customto yield a crude product which
  9. customis purified by flash column chromatography (10% ethyl acetate/hexane to 70% ethyl acetate/hexane eluant)

출처 및 근거

ORD 기록
ord-87d2f789a9394e3680500b84f128f3e8
출처 데이터셋
uspto-grants-2014_10
특허 번호
US08865623B2

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