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Water → HCID 90004151, 화합물

HRID 587854
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HRID 587854 반응식
[O:1]=[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH2:5][C@@H:4]([C:12]([OH:14])=[O:13])[CH2:3]1.[C:15]([O-])([O-])=O.[K+].[K+].CI.O>CN(C=O)C>[O:1]=[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH2:5][C@@H:4]([C:12]([O:14][CH3:15])=[O:13])[CH2:3]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 7000055HCID 7000055, 화합물

생성물 1

HCID 90004151HCID 90004151, 화합물수율 83.8%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
온도
25 °C

실험 절차

To the stirred solution of (R)-4-oxo-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid (5.0 g, 26.3 mmol), K2CO3 (10.90 g, 79 mmol) and methyl iodide (6.58 ml, 105 mmol) was added in DMF (50 mL) and stirred for overnight at 25° C. Water was added (130 mL) and extracted with ethyl acetate (2×30 mL). The organic phase was washed with aq. Sodium bicarbonate solution (2×20 mL), dried over Na2SO4 and filtered. The clear organic phase was evaporated in vacuo to get title compound (4.5 g) m/z 204.09.

후처리

  1. extractionextracted with ethyl acetate (2×30 mL)
  2. washThe organic phase was washed with aq. Sodium bicarbonate solution (2×20 mL)
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. customThe clear organic phase was evaporated in vacuo

출처 및 근거

ORD 기록
ord-c6e522bb6ad64d94b414fe42a9133cd5
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09227919B2

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