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Hydrochloric Acid → HCID 18679819, 화합물

HRID 1633568
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HRID 1633568 반응식
[C:1]([C:5]1[CH:6]=[C:7]([CH2:12][CH2:13][C:14]([OH:16])=[O:15])[CH:8]=[CH:9][C:10]=1[OH:11])([CH3:4])([CH3:3])[CH3:2].[CH:17]([CH:19]=O)=[O:18].Cl>C(O)(=O)C>[C:1]([C:5]1[C:10]2[O:11][C:17](=[O:18])[CH2:19][C:9]=2[CH:8]=[C:7]([CH2:12][CH2:13][C:14]([OH:16])=[O:15])[CH:6]=1)([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 7860GlyoxalHCID 54637793-(3-tert-Butyl-4-hydroxyphenyl)propanoic acid

생성물 1

HCID 18679819HCID 18679819, 화합물

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

66.7 g (0.3 mol) of 3-(3-tert-butyl-4-hydroxy-phenyl)-propionic acid (prepared analogously to the method described in JP-A2-63/227542) in 58 g (0.4 mol) of aqueous glyoxal solution (40% by weight) and 3 ml of hydrochloric acid (32% by weight) are heated at reflux in 200 ml of acetic acid for 6 hours. The mixture is then poured into 600 ml of ice-water and the precipitate is filtered off. The filter residue is washed with water and then dried at 60° C. g. Recrystallisation from toluene results in 54.3 g (69% of theory) of 3-(7-tert-butyl-2-oxo-2,3-dihydro-benzofuran-5-yl)-propionic acid. Melting point 167-169° C.

후처리

  1. filtrationthe precipitate is filtered off
  2. washThe filter residue is washed with water
  3. customdried at 60° C.
  4. customRecrystallisation from toluene
  5. customresults in 54.3 g (69% of theory) of 3-(7-tert-butyl-2-oxo-2,3-dihydro-benzofuran-5-yl)-propionic acid

출처 및 근거

ORD 기록
ord-e75aed4e99ff48a78f60cd2fd905994e
출처 데이터셋
uspto-grants-2003_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06503937B1

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