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Ethanol → Ethyl 2,3-Dihydrobenzofuran-5-ylacetate

HRID 868621
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인쇄 미리보기

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HRID 868621 반응식
[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][C:11]([OH:13])=[O:12])=[CH:9][C:4]=2[CH2:3][CH2:2]1.[C:14]1(C)C=CC=C[CH:15]=1.C(O)C.S(=O)(=O)(O)O>O.C(OCC)(=O)C.O>[O:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12])=[CH:9][C:4]=2[CH2:3][CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 702EthanolHCID 1118Sulfuric AcidHCID 1140TolueneHCID 27374552,3-Dihydro-5-benzofuranacetic acid

생성물 1

HCID 13704383Ethyl 2,3-Dihydrobenzofuran-5-ylacetate

시약·촉매·용매 2

HCID 962Water용매HCID 22728543

실험 절차

2,3-dihydrobenzofuran-5-ylacetic acid (5.4 g) was heated at reflux in a solution of toluene (200 ml), ethanol (20 ml) and concentrated sulfuric acid (0.5 ml) with the azeotropic removal of water. When the reaction was complete, approximately 6 hours, the mixture was added to water/ethyl acetate and extracted with ethyl acetate. The organic extracts were combined and washed with 10% sodium carbonate, dried over sodium sulfate and the solvent evaporated to give the title compound as an oil.

후처리

  1. extractionextracted with ethyl acetate
  2. washwashed with 10% sodium carbonate
  3. dry with materialdried over sodium sulfate
  4. customthe solvent evaporated

출처 및 근거

ORD 기록
ord-995e1e9946c646fb8a03efc05e7ac0b9
출처 데이터셋
uspto-grants-1988_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04780480

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Water ethylacetate
용매