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Triethylamine → HCID 87312108, 화합물

HRID 982819
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HRID 982819 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[CH2:9][CH2:10][CH2:11][OH:12].C(N(CC)CC)C.[CH3:20][S:21](Cl)(=[O:23])=[O:22]>C(Cl)Cl.[Cl-].[Na+].O>[CH3:20][S:21]([O:12][CH2:11][CH2:10][CH2:9][C:3]1[C:2]([Cl:1])=[CH:7][CH:6]=[CH:5][C:4]=1[Cl:8])(=[O:23])=[O:22]
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참가 물질

6

반응물 3

HCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 219565353-(2,6-Dichlorophenyl)propan-1-ol

생성물 1

HCID 87312108HCID 87312108, 화합물

시약·촉매·용매 2

HCID 6344Dichloromethane용매HCID 57417360Sodium chloride; water용매

실험 절차

To a solution of 3-(2,6-dichlorophenyl)-1-propanol (125 mg, 0.61 mmol) and triethylamine (123 mg, 1.22 mmol) in methylene chloride (3 mL), methanesulfonyl chloride (105 mg, 0.915 mmol) was added under ice cooling, followed by stirring at room temperature for 2 hours. Brine was added to the reaction mixture. The organic layer was allowed to separate, was collected, and was then dried over anhydrous sodium sulfate. Subsequent to concentration under reduced pressure, the residue was purified by chromatography on a silica gel column (hexane/ethyl acetate=10/1) to yield the title compound as a pale yellow syrupy substance (yield: quantitative).

후처리

  1. customto separate
  2. customwas collected
  3. dry with materialwas then dried over anhydrous sodium sulfate
  4. concentrationSubsequent to concentration under reduced pressure
  5. customthe residue was purified by chromatography on a silica gel column (hexane/ethyl acetate=10/1)

출처 및 근거

ORD 기록
ord-c0a06165811a46a083d7ab12507ddb0f
출처 데이터셋
uspto-grants-2005_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06861428B2

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