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Acetic Acid → 6-(3-bromo-2-hydroxypropoxy)-3,4-dihydroquinolin-2(1H)-one

HRID 1023179
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반응식

HRID 1023179 반응식
[O:1]1[CH2:3][CH:2]1[CH2:4][O:5][C:6]1[CH:7]=[C:8]2[C:13](=[CH:14][CH:15]=1)[NH:12][C:11](=[O:16])[CH2:10][CH2:9]2.C(O)(=O)C.[Br-:21].[Li+]>C1COCC1>[Br:21][CH2:3][CH:2]([OH:1])[CH2:4][O:5][C:6]1[CH:7]=[C:8]2[C:13](=[CH:14][CH:15]=1)[NH:12][C:11](=[O:16])[CH2:10][CH2:9]2
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참가 물질

5

반응물 3

HCID 176Acetic AcidHCID 82050Lithium BromideHCID 145174016-(Oxiran-2-ylmethoxy)-3,4-dihydroquinolin-2(1H)-one

생성물 1

HCID 866804246-(3-bromo-2-hydroxypropoxy)-3,4-dihydroquinolin-2(1H)-one수율 10,085.3%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a stirred solution of 6-(oxiran-2-ylmethoxy)-3,4-dihydroquinolin-2(1H)-one (0.2 g, 0.909 mmol) in dry THF (5 mL) was added acetic acid (0.162 g, 2.272 mmol) and lithium bromide (0.118 g, 1.363 mmol). The reaction mixture was stirred at room temperature for 3 h. The reaction mixture was concentrated to remove solvent and water was added (25 mL). The solid was filtered and dried to give crude 6-(3-bromo-2-hydroxypropoxy)-3,4-dihydroquinolin-2(1H)-one as an off-white solid (0.25 g, 91.675 mmol). LCMS: RT 0.65 min; LCMS (ES-API), m/z 300.0 (M+H).

후처리

  1. concentrationThe reaction mixture was concentrated
  2. customto remove solvent and water
  3. additionwas added (25 mL)
  4. filtrationThe solid was filtered
  5. customdried

출처 및 근거

ORD 기록
ord-867f36281d0c46f3aa3ba206c3c75461
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08722670B2

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