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Potassium Carbonate → HCID 66696682, 화합물

HRID 1672577
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HRID 1672577 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[C:10]([F:13])([F:12])[F:11])[CH:5]=[O:6].[N+:14]([CH:16](S(C1C=CC(C)=CC=1)(=O)=O)[CH3:17])#[C-:15].C([O-])([O-])=O.[K+].[K+]>CO>[Cl:1][C:2]1[CH:3]=[C:4]([C:5]2[O:6][CH:15]=[N:14][C:16]=2[CH3:17])[CH:7]=[CH:8][C:9]=1[C:10]([F:11])([F:12])[F:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 110528851-(1-Isocyanoethanesulfonyl)-4-methylbenzeneHCID 190312873-Chloro-4-(trifluoromethyl)benzaldehyde

생성물 1

HCID 66696682HCID 66696682, 화합물수율 85.4%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A mixture of Example 45A (2.84 g, 13.6 mmol), 1-(1-isocyanoethylsulfonyl)-4-methylbenzene (2.85 g, 13.6 mmol), and K2CO3 (2.26 g, 16.3 mmol) in MeOH (70 mL) was heated to reflux. After 2 hr the reaction mixture was cooled to ambient temperature, and the volatiles were evaporated at reduced pressure. The residue was partitioned between Et2O and H2O. The separated aqueous layer was extracted with Et2O, and the combined organic phase was washed with brine, dried (Na2SO4), filtered, and concentrated in vacuo. Flash chromatography (Analogix® Intelliflash 280; 10% to 30% EtOAc/hexanes eluant; SF40-150 g column) yielded 3.04 g (85%) of the title compound as a white solid. 1H NMR (300 MHz, DMSO-d6) δ 8.48 (s, 1H), 7.96 (d, J=8.4, 1H), 7.87 (s, 1H), 7.78 (dd, J=8.3, 0.8, 1H), 2.43 (s, 3H). MS (DCI+) m/z 262 (M+H).

후처리

  1. customthe volatiles were evaporated at reduced pressure
  2. customThe residue was partitioned between Et2O and H2O
  3. extractionThe separated aqueous layer was extracted with Et2O
  4. washthe combined organic phase was washed with brine
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-6d77e042616e425fb599eda100f9b99f
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07998993B2

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