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Cesium carbonate → 2-(4-Hydroxy-naphthalen-2-yloxy)-2-methyl-propionic acid ethyl ester

HRID 1727013
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HRID 1727013 반응식
[CH2:1]([O:3][C:4](=[O:28])[C:5]([CH3:27])([O:7][C:8]1[CH:17]=[C:16]([O:18]COCC[Si](C)(C)C)[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:9]=1)[CH3:6])[CH3:2].C[Si](C)(C)CCOCOC1C2C(=CC=CC=2)C=C(O)C=1.BrC(C)(C)C(OCC)=O.C(=O)([O-])[O-].[Cs+].[Cs+].Cl.CCO>CCO>[CH2:1]([O:3][C:4](=[O:28])[C:5]([O:7][C:8]1[CH:17]=[C:16]([OH:18])[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:9]=1)([CH3:27])[CH3:6])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 10796Cesium carbonateHCID 11745Propanoic acid, 2-bromo-2-methyl-, ethyl esterHCID 21887872Ethanol hydrochlorideHCID 690373392-Methyl-2-[4-(2-trimethylsilanyl-ethoxymethoxy)-naphthalen-2-yloxy]-propionic acid ethyl esterHCID 690383454-(2-Trimethylsilanyl-ethoxymethoxy)-naphthalen-2-ol

생성물 1

HCID 69038379
2-(4-Hydroxy-naphthalen-2-yloxy)-2-methyl-propionic acid ethyl ester
수율 99.1%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

1.58 g (3.90 mmol) of 2-methyl-2-[4-(2-trimethylsilanyl-ethoxymethoxy)-naphthalen-2-yloxy]-propionic acid ethyl ester (prepared from 4-(2-trimethylsilanyl-ethoxymethoxy)-naphthalen-2-ol, ethyl bromoisobutyrate, cesium carbonate, in analogy to the procedure described in example 14B] was dissolved in 20 ml of EtOH; then, 1.95 ml of HCl/EtOH-solution (6 molar) was added drop by drop. After 7 hours stirring at room temperature, the solvent was removed by evaporation and the residue was partitioned between water and MeCl2. The organic phase was separated, washed with water, dried (MgSO4) and evaporated. The crude product was purified by chromatography over silica gel with a gradient of AcOEt/heptane to give 1.06 g of pure 2-(4-hydroxy-naphthalen-2-yloxy)-2-methyl-propionic acid ethyl ester as light brown oil.

후처리

  1. customthe solvent was removed by evaporation
  2. customthe residue was partitioned between water and MeCl2
  3. customThe organic phase was separated
  4. washwashed with water
  5. dry with materialdried (MgSO4)
  6. customevaporated
  7. customThe crude product was purified by chromatography over silica gel with a gradient of AcOEt/heptane

출처 및 근거

ORD 기록
ord-03840e410ddc48febfccfc35bb8331ff
출처 데이터셋
uspto-grants-2009_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07495001B2

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