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Water → HCID 20080796, 화합물

HRID 1653838
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HRID 1653838 반응식
[Cl:1][C:2]1[CH:18]=[CH:17][C:5]([O:6][C:7]2[CH:12]=[CH:11][C:10]([CH2:13][C:14](=[O:16])[CH3:15])=[CH:9][CH:8]=2)=[CH:4][CH:3]=1.O.CC[O:22][CH2:23][CH3:24].[C:25](OC(=O)C)(=O)[CH3:26]>>[Cl:1][C:2]1[CH:18]=[CH:17][C:5]([O:6][C:7]2[CH:12]=[CH:11][C:10]([C:13]3[C:23](=[O:22])[CH:24]=[C:25]([CH3:26])[O:16][C:14]=3[CH3:15])=[CH:9][CH:8]=2)=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 962WaterHCID 3283Diethyl EtherHCID 7918Acetic Anhydride2회HCID 18000323HCID 18000323, 화합물

생성물 1

HCID 20080796HCID 20080796, 화합물

실험 절차

A solution of 4-(4-chlorophenoxy)phenylpropan-2-one (26 g) in acetic anhydride (100 ml) was added, over 5 min, to a vigorously stirred mixture of polyphosphoric acid (200 g) and acetic anhydride (100 ml) at 80°. After stirring for 30 min the mixture was poured into water (1 liter) and extracted with toluene (2×500 ml). The combined extracts were washed with water then satd. aq. sodium bicarbonate, dried over magnesium sulphate and evaporated to give an oil. Trituration with ether gave a yellow solid, which was recrystallised from carbon tetrachloride to afford the title compound (14.64 g), m.p. 150°-152°, NMR δH (CDCl3) 6.95-7.4 (8H, m), 6.2 (1H, s), 2.3 (3H, s), 2.2 (3H, s).

후처리

  1. extractionextracted with toluene (2×500 ml)
  2. washThe combined extracts were washed with water
  3. dry with materialaq. sodium bicarbonate, dried over magnesium sulphate
  4. customevaporated
  5. customto give an oil
  6. customwas recrystallised from carbon tetrachloride

출처 및 근거

ORD 기록
ord-7bff8d2e4b594381b738e592b0329dba
출처 데이터셋
uspto-grants-1995_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05403934

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