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Sodium Hydroxide → 2-Nitro-5-(2,4,6-trichlorophenoxy)benzoic acid

HRID 894933
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HRID 894933 반응식
[N+:1]([C:4]1[CH:14]=[CH:13][C:12]([O:15][C:16]2[C:21]([Cl:22])=[CH:20][C:19]([Cl:23])=[CH:18][C:17]=2[Cl:24])=[CH:11][C:5]=1[C:6]([O:8]CC)=[O:7])([O-:3])=[O:2].[OH-].[Na+]>C(O)C.O>[N+:1]([C:4]1[CH:14]=[CH:13][C:12]([O:15][C:16]2[C:17]([Cl:24])=[CH:18][C:19]([Cl:23])=[CH:20][C:21]=2[Cl:22])=[CH:11][C:5]=1[C:6]([OH:8])=[O:7])([O-:3])=[O:2]
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참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 13013678Ethyl 2-nitro-5-(2,4,6-trichlorophenoxy)benzoate

생성물 1

HCID 130136912-Nitro-5-(2,4,6-trichlorophenoxy)benzoic acid수율 66.9%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

실험 절차

The product from paragraph (a) (6.86 g) in ethanol (50 ml) was heated and stirred with a solution of sodium hydroxide (0.8 g) in water (10 ml) at 60°-70° C. for 4 hours. The mixture was then cooled and the ethanol removed under reduced pressure. The residue was diluted to 100 ml with water and brought to pH 2 with concentrated hydrochloric acid. The solid which separated was collected and recrystallised from toluene to give the required benzoic acid derivative (4.26 g) with a melting point of 192°-192.5° C.

후처리

  1. temperatureThe mixture was then cooled
  2. customthe ethanol removed under reduced pressure
  3. additionThe residue was diluted to 100 ml with water
  4. customThe solid which separated
  5. customwas collected
  6. customrecrystallised from toluene

출처 및 근거

ORD 기록
ord-0285d12a4b87462aa2c6ac0498018813
출처 데이터셋
uspto-grants-1981_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04285723

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