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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → HCID 23215434, 화합물

HRID 1894144
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HRID 1894144 반응식
[F:1][CH2:2][O:3][C:4]1[CH:9]=[CH:8][C:7](C(=O)C)=[CH:6][CH:5]=1.C1C=C(Cl)C=C(C(OO)=[O:21])C=1.[Li+].[OH-].Cl>ClCCl.C1COCC1.CO.O>[F:1][CH2:2][O:3][C:4]1[CH:9]=[CH:8][C:7]([OH:21])=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 3939Lithium HydroxideHCID 70297m-Chloroperbenzoic acidHCID 109758681-[4-(Fluoromethoxy)phenyl]ethanone

생성물 1

HCID 23215434HCID 23215434, 화합물수율 102.8%

시약·촉매·용매 2

HCID 6344Dichloromethane용매
HCID 21892291
Methanol tetrahydrofuran water
용매

실험 절차

To a solution of 1-(4-fluoromethoxy-phenyl)-ethanone (1.5 g; 8.9 mmol) in dichloromethane (30 mL) was added mCPBA (4.0 g; 17.8 mmol). The resulting mixture was stirred at room temperature for 4 h, then washed with saturated NaHCO3 (3×). The organic layer was dried over Na2SO4, concentrated under reduced pressure to give the crude material (3.77 g). The crude material (3.77 g) was dissolved in THF/MeOH/H2O (5/5/5 mL), then treated with LiOH (4.0 g; 108 mmol) at room temperature for 4 h. The reaction mixture was acidified with 2N HCl solution to pH 5. The mixture was extracted with EtOAc (3×). The organic phases were combined, dried over Na2SO4 and concentrated under reduced pressure to afford the title compound (1.3 g). This compound was used directly without further purification.

후처리

  1. washwashed with saturated NaHCO3 (3×)
  2. dry with materialThe organic layer was dried over Na2SO4
  3. concentrationconcentrated under reduced pressure
  4. customto give the crude material (3.77 g)
  5. extractionThe mixture was extracted with EtOAc (3×)
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-3264530ed5e044af8685708a859f46d6
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08513271B2

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