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Sodium Bicarbonate → 1-[2-Hydroxy-5-(2-hydroxyethyl)phenyl]-ethanone

HRID 1438977
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HRID 1438977 반응식
C([O:4][CH2:5][CH2:6][C:7]1[CH:12]=[CH:11][C:10]([OH:13])=[C:9]([C:14](=[O:16])[CH3:15])[CH:8]=1)(=O)C.C(=O)(O)[O-].[Na+]>C(O)C.O>[C:14]([C:9]1[CH:8]=[C:7]([CH:12]=[CH:11][C:10]=1[OH:13])[CH2:6][CH2:5][OH:4])(=[O:16])[CH3:15]
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참가 물질

5

반응물 2

HCID 516892Sodium BicarbonateHCID 127698062-(3-Acetyl-4-hydroxyphenyl)ethyl acetate

생성물 1

HCID 127698071-[2-Hydroxy-5-(2-hydroxyethyl)phenyl]-ethanone수율 108.1%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

실험 절차

A solution of 2-(3-acetyl-4-hydroxyphenyl)ethyl acetate (35.7g) in ethanol (400 ml), and sodium bicarbonate (42g) in water (200 mls) was refluxed for 81/2 hours. The ethanol was removed on a `Rotavapor` and the residue was extracted with ether (3x). The combined ethereal extracts were washed with water, sodium bicarbonate solution, saturated brine solution, dried over anhydrous magnesium sulphate, and evaporated to yield a red oil (31.3g). The oil was recrystallised from hexane and ether (4:1) to yield the product as a pale yellow crystalline solid (18.3g). The mother liquors were concentrated and an additional batch of product was obtained as a pale yellow crystalline solid (9.3g).

후처리

  1. customThe ethanol was removed on a `Rotavapor` and the residue
  2. extractionwas extracted with ether (3x)
  3. washThe combined ethereal extracts were washed with water, sodium bicarbonate solution, saturated brine solution
  4. dry with materialdried over anhydrous magnesium sulphate
  5. customevaporated

출처 및 근거

ORD 기록
ord-f6a87caa0d804900acedf86b9a0dff83
출처 데이터셋
uspto-grants-1977_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04057641

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