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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium Hydroxide → 3-(3,5-Dichlorophenyl)acrylic acid

HRID 1480421
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HRID 1480421 반응식
[Cl:1][C:2]1[CH:3]=[C:4](/[CH:9]=[CH:10]/[C:11]([O:13]C)=[O:12])[CH:5]=[C:6]([Cl:8])[CH:7]=1.[OH-].[Na+]>C1COCC1>[Cl:1][C:2]1[CH:3]=[C:4](/[CH:9]=[CH:10]/[C:11]([OH:13])=[O:12])[CH:5]=[C:6]([Cl:8])[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 69907122Methyl (E)-3-(3,5-dichlorophenyl)acrylate

생성물 1

HCID 64421483-(3,5-Dichlorophenyl)acrylic acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To (E)-methyl 3-(3,5-dichlorophenyl)acrylate (step 1) (2 g, 8.66 mmol) in THF (35 ml) was added 2M NaOH (12.98 ml, 26.0 mmol) and the reaction mixture was stirred at RT overnight. The solvent was removed under reduced pressure and the residue was dissolved in water and washed with EtOAc. The aqueous portion was acidified to pH 4 using 1M HCl and extracted with DCM. The organic portion was dried using a phase separating column and the solvent removed under reduced pressure to afford the title compound as a white solid;

후처리

  1. customThe solvent was removed under reduced pressure
  2. dissolutionthe residue was dissolved in water
  3. washwashed with EtOAc
  4. extractionextracted with DCM
  5. customThe organic portion was dried
  6. customseparating column
  7. customthe solvent removed under reduced pressure

출처 및 근거

ORD 기록
ord-caab693769ac4e62b8ba72e0eb1f1095
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09409895B2

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