Potassium Carbonate → Methyl 2-(2-bromo-5-phenylthiophen-3-yl)-2-(tert-butoxy)acetate

HRID 590994노트

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HRID 590994 반응식
[Br:1][C:2]1[S:3][C:4]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[CH:5][C:6]=1[CH:7]([OH:12])[C:8]([O:10][CH3:11])=[O:9].Cl(O)(=O)(=O)=O.C(=O)([O-])[O-].[K+].[K+]>C(OC(C)(C)C)(=O)C>[Br:1][C:2]1[S:3][C:4]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[CH:5][C:6]=1[CH:7]([O:12][C:6]([CH3:7])([CH3:5])[CH3:2])[C:8]([O:10][CH3:11])=[O:9]

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 24247Perchloric AcidHCID 70818099Methyl 2-(2-bromo-5-phenylthiophen-3-yl)-2-hydroxyacetate

생성물 1

HCID 70819299Methyl 2-(2-bromo-5-phenylthiophen-3-yl)-2-(tert-butoxy)acetate수율 173.9%

시약·촉매·용매 1

HCID 10908tert-Butyl acetate용매

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온도
0 °C

실험 절차

Methyl 2-(2-bromo-5-phenylthiophen-3-yl)-2-hydroxyacetate (11h) (75 mg, 0.23 mmol) was dissolved in tert-butyl acetate (8.6 mL) at 0° C. and 70% perchloric acid (1.1 mL) was rapidly added. The mixture was stirred at 0° C. for 30 minutes then poured in a saturated solution of potassium carbonate. Layers were separated. The aqueous layer was extracted with ethyl acetate (2×15 mL). The organic layers were washed with brine (8 mL), dried over sodium sulfate and concentrated in vacuo to provide the desired product (11i) (77 mg, 0.20 mmol, 87%) which was used without further purification.

후처리

  1. customLayers were separated
  2. extractionThe aqueous layer was extracted with ethyl acetate (2×15 mL)
  3. washThe organic layers were washed with brine (8 mL)
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-e0924bf67ed6436db3850b3eeff8de43
출처 데이터셋
uspto-grants-2016_01
특허 번호
US09238026B2

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