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Sodium Hydroxide → 2,4-Dibromo-3-(ethylcarbonylmethoxy)benzoic acid

HRID 585326
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HRID 585326 반응식
[Br:1][C:2]1[C:12]([O:13][CH2:14][C:15]([CH2:17][CH3:18])=[O:16])=[C:11]([Br:19])[CH:10]=[CH:9][C:3]=1[C:4]([O:6]CC)=[O:5].[OH-].[Na+]>C1COCC1.O>[Br:1][C:2]1[C:12]([O:13][CH2:14][C:15]([CH2:17][CH3:18])=[O:16])=[C:11]([Br:19])[CH:10]=[CH:9][C:3]=1[C:4]([OH:6])=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 22340637Ethyl 2,4-dibromo-3-(ethylcarbonylmethoxy)benzoate

생성물 1

HCID 223406262,4-Dibromo-3-(ethylcarbonylmethoxy)benzoic acid

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매

실험 절차

1.280 g (3.20 mmol) of ethyl 2,4-dibromo-3-(ethylcarbonylmethoxy)benzoate were dissolved in 15 ml of THF and 15 ml of water, and 0.143 g (3.6 mmol) of NaOH was added. The mixture was stirred at RT for 12 h and then evaporated to dryness. The residue was taken up in water, and 6 N HCl was added. The resulting precipitate was filtered off with suction and dried. This gave 2,4-dibromo-3-(ethylcarbonylmethoxy)benzoic acid in the form of a white solid.

후처리

  1. customevaporated to dryness
  2. addition6 N HCl was added
  3. filtrationThe resulting precipitate was filtered off with suction
  4. customdried

출처 및 근거

ORD 기록
ord-18e9cdd5b8784b7fa7075667cef17e09
출처 데이터셋
uspto-grants-2005_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06930208B2

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