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Hydrochloric Acid → ({1-[(3-Hydroxyphenyl)ethynyl]-2-naphthyl}oxy)acetic acid

HRID 2390369
ノート
印刷プレビュー

反応式

HRID 2390369 の反応式
C([O:5][C:6](=[O:20])[CH2:7][O:8][C:9]1[CH:18]=[CH:17][C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[C:10]=1Br)(C)(C)C.[OH:21][C:22]1[CH:23]=[C:24]([C:28]#[CH:29])[CH:25]=[CH:26][CH:27]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N1CCCCC1.Cl>O.CC(C)=O.C(Cl)Cl.O1CCOCC1.[Pd](Cl)Cl>[OH:21][C:22]1[CH:23]=[C:24]([C:28]#[C:29][C:10]2[C:11]3[C:16](=[CH:15][CH:14]=[CH:13][CH:12]=3)[CH:17]=[CH:18][C:9]=2[O:8][CH2:7][C:6]([OH:5])=[O:20])[CH:25]=[CH:26][CH:27]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

11

反応物 5

HCID 313Hydrochloric AcidHCID 8082PiperidineHCID 11776TriphenylphosphineHCID 139144m-EthynylphenolHCID 58522023tert-Butyl[(1-bromo-2-naphthyl)oxy]acetate2 回

生成物 1

HCID 46865199({1-[(3-Hydroxyphenyl)ethynyl]-2-naphthyl}oxy)acetic acid

試薬・触媒・溶媒 5

HCID 24290Palladium Chloride触媒HCID 180Acetone溶媒HCID 962Water溶媒HCID 6344Dichloromethane溶媒HCID 312751,4-Dioxane溶媒

反応条件

温度
60 °C

実験手順

A mixture of (1-bromo-naphthalen-2-yloxy)-acetic acid tert-butyl ester (Intermediate 217, 125 mg; 0.37 mmol), 3-hydroxyphenylacetylene (53 mg; 0.44 mmol), palladium(II) chloride (3.3 mg; 0.02 mmol), triphenylphosphine (10 mg; 0.04 mmol) and piperidine (73 μl; 0.74 mmol) in distilled water (1.1 ml) and Acetone (1.4 ml) was stirred overnight at 60° C. The reaction mixture was extracted by EtOAc and the organic phases was dried over MgSO4, concentrated to dryness and purified by preparative HPLC. The intermediate obtained was diluted in DCM (1 ml) and treated with a 4 M solution of HCl in dioxane (930 μl). After stirring overnight, the reaction mixture was concentrated to dryness and purified by preparative HPLC to afford the title compound as a beige solid.

後処理

  1. extractionThe reaction mixture was extracted by EtOAc
  2. dry with materialthe organic phases was dried over MgSO4
  3. concentrationconcentrated to dryness
  4. custompurified by preparative HPLC
  5. customThe intermediate obtained
  6. stirringAfter stirring overnight
  7. concentrationthe reaction mixture was concentrated to dryness
  8. custompurified by preparative HPLC

出典と根拠

ORDレコード
ord-96953d28d6ea48d583122c2b837410c7
出典データセット
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08273769B2

反応ノート

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