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Dichloromethane → 3-Acetoxy-8-methoxy quinoline

HRID 399746
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HRID 399746 반응식
[OH:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][C:6]=2[O:12][CH3:13].C(N(CC)CC)C.ClCCl.[C:24](Cl)(=[O:26])[CH3:25]>O>[C:24]([O:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][C:6]=2[O:12][CH3:13])(=[O:26])[CH3:25]
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참가 물질

6

반응물 4

HCID 6344DichloromethaneHCID 6367Acetyl chlorideHCID 8471TriethylamineHCID 110843893-Quinolinol, 8-methoxy-2회

생성물 1

HCID 189450663-Acetoxy-8-methoxy quinoline

시약·촉매·용매 1

HCID 962Water용매

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온도
0 °C

실험 절차

175 mg of 3-hydroxy-8-methoxy quinoline [compound (V)] prepared in example 6 and 132 mg of triethyl amine were added to 10 ml of dichloromethane. After cooled to 0° C., 0.1 ml of acetyl chloride was slowly added dropwise. The solution was agitated for 1 hour, and water was added to the solution. The solution was extracted with dichloromethane and washed with water. The dichloromethane layer was dried with anhydrous magnesium sulfate. The dichloromethane was removed by vacuum distillation to give 195 mg of 3-acetoxy-8-methoxy quinoline as an oil.

후처리

  1. extractionThe solution was extracted with dichloromethane
  2. washwashed with water
  3. dry with materialThe dichloromethane layer was dried with anhydrous magnesium sulfate
  4. customThe dichloromethane was removed by vacuum distillation

출처 및 근거

ORD 기록
ord-39fa172cb72648fe9375f59f6e330b81
출처 데이터셋
uspto-grants-1998_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05824689

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