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Diethyl Ether → HCID 12641422, 화합물

HRID 2422011
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HRID 2422011 반응식
[C:1]1([CH3:12])[CH:6]=[C:5]([CH3:7])[CH:4]=[C:3]([CH3:8])[C:2]=1[CH2:9][CH:10]=[O:11].C[Mg+].[Br-].[CH3:16]COCC>C1COCC1>[C:3]1([CH3:8])[CH:4]=[C:5]([CH3:7])[CH:6]=[C:1]([CH3:12])[C:2]=1[CH2:9][CH:10]([OH:11])[CH3:16]
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참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 3003822-(2,4,6-Trimethylphenyl)acetaldehydeHCID 178418689HCID 178418689, 화합물

생성물 1

HCID 12641422HCID 12641422, 화합물수율 68.3%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Mesitylacetaldehyde (0.68 g, 4.19 mmol) was dissolved in THF (5.0 mL, dry) and MeMgBr in Et2O (3.0M, 0.75 g, 6.29 mmol)) was added slowly at 0° C. The cooling bath was removed and the reaction mixture was stirred at rt for 4.5 h. The mixture was cooled to 0° C. and excess Grignard reagent was hydrolyzed with HCl (1N). The mixture was diluted with water and extracted with Et2O. The organic layer was dried over Na2SO4, evaporated and the residue was purified by column chromatography on silica gel using MTBE, heptane and DCM as eluant giving the title compound (0.51 g, 61%). 1H NMR (CDCl3, 500 MHz) δ 6.88-6.85 (m, 2H), 4.08-3.99 (m, 1H), 2.87-2.72 (m, 2H), 2.32 (s, 6H), 2.26 (s, 3H), 1.29 (d, 3H).

후처리

  1. customThe cooling bath was removed
  2. temperatureThe mixture was cooled to 0° C.
  3. additionThe mixture was diluted with water
  4. extractionextracted with Et2O
  5. dry with materialThe organic layer was dried over Na2SO4
  6. customevaporated
  7. customthe residue was purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-931356e574354a9da4ba8cc8c2c01600
출처 데이터셋
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07960380B2

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