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Bromide ion → HCID 58136965, 화합물

HRID 657967
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HRID 657967 반응식
[OH:1][C:2]1[CH:3]=[C:4]([C:14](=[O:16])[CH3:15])[CH:5]=[C:6]([S:8]([F:13])([F:12])([F:11])([F:10])[F:9])[CH:7]=1.Br[CH2:18][CH:19]([O:21][CH3:22])C.[H-].[Na+].[Br-]>CN(C=O)C.CC(=O)OCC>[CH3:22][O:21][CH2:19][CH2:18][O:1][C:2]1[CH:3]=[C:4]([C:14](=[O:16])[CH3:15])[CH:5]=[C:6]([S:8]([F:13])([F:9])([F:10])([F:11])[F:12])[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 259Bromide ionHCID 24758Sodium hydrideHCID 524021Propane, 1-bromo-2-methoxy-HCID 58136805HCID 58136805, 화합물

생성물 1

HCID 58136965HCID 58136965, 화합물수율 78.4%

시약·촉매·용매 2

HCID 6228Dimethylformamide용매2회
HCID 8857
Ethyl Acetate
용매

실험 절차

1-[3-Hydroxy-5-(pentafluorosulfanyl)phenyl]ethanone (O3.050; 700 mg) and 1-bromo-2-methoxypropane (490 mg) were dissolved in DMF (10 ml), and sodium hydride (77 mg) was added. After stirring at RT for 2 h, further bromide (100 μl) was added and the mixture was heated to 50° C. for 6 h. Then the DMF was drawn off and the residue was taken up in EA, washed with water, dried, filtered and concentrated. 670 mg of the title compound were obtained. LC-MS rt: 1.71 min [M+H]+: 335.1 (met. a)

후처리

  1. temperaturethe mixture was heated to 50° C. for 6 h
  2. washwashed with water
  3. customdried
  4. filtrationfiltered
  5. concentrationconcentrated

출처 및 근거

ORD 기록
ord-69ffbb5b4dc845cd9a1138cb14eaf89f
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08076336B2

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