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Acetonitrile → HCID 86646688, 화합물

HRID 1677506
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HRID 1677506 반응식
CC1(C=O)CC[C:4]2([O:11][CH2:10][C:9]([CH3:13])([CH3:12])[CH2:8][O:7]2)C1.[C:16]([O-:19])([O-])=O.[K+].[K+].BrCCCCBr.C[C:29]#[N:30]>O>[CH3:4][O:11][CH2:10][C:9]([CH3:12])([CH3:13])[C:8]([N:30]([O:19][CH3:16])[CH3:29])=[O:7]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

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HCID 6342AcetonitrileHCID 80561,4-Dibromobutane2회HCID 11430Potassium CarbonateHCID 595406622,8,8-Trimethyl-6,10-dioxa-spiro[4.5]decane-2-carbaldehyde

생성물 1

HCID 86646688HCID 86646688, 화합물

시약·촉매·용매 1

HCID 962Water용매

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온도
110 °C

실험 절차

Step 3—A mixture of 2 (0.9 g, 3.912 mmol), K2CO3 (0.595 g, 4.303 mmol) and 1,4-dibromobutane (0.49 mL, 4.108 mmol) in 14 mL of CH3CN and 1 mL of H2O was stirred at 110° C. for 30 minutes under microwave irradiation before being cooled to RT. 0.5 more equivalents of 1,4-dibromobutane were added and the resulting mixture was stirred at 110° C. for 30 minutes under microwave irradiation a second time before being cooled to RT. The reaction mixture was extracted twice with DCM. The combined organic layers were dried (Na2SO4), filtered, and evaporated. The residue was purified by SiO2 chromatography (hexanes/EtOAc 0-8% EtOAc) to give 0.25 g of 3: 3-bromo-5-pyrrolidin-1-yl-benzoic acid methyl ester (22% yield).

후처리

  1. temperaturebefore being cooled to RT
  2. stirringthe resulting mixture was stirred at 110° C. for 30 minutes under microwave irradiation a second time
  3. temperaturebefore being cooled to RT
  4. extractionThe reaction mixture was extracted twice with DCM
  5. dry with materialThe combined organic layers were dried (Na2SO4)
  6. filtrationfiltered
  7. customevaporated
  8. customThe residue was purified by SiO2 chromatography (hexanes/EtOAc 0-8% EtOAc)

출처 및 근거

ORD 기록
ord-a7fe6812273c45c6aed870a8ad795090
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08008298B2

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