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Hydrochloric Acid → 3-(5-Dimethylcarbamoyl-pent-1-ynyl)-benzoic acid

HRID 2067168
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반응식

HRID 2067168 반응식
C([O:3][C:4](=[O:21])[C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]#[C:12][CH2:13][CH2:14][CH2:15][C:16](=[O:20])[N:17]([CH3:19])[CH3:18])[CH:6]=1)C.[OH-].[Na+].Cl>>[CH3:19][N:17]([CH3:18])[C:16]([CH2:15][CH2:14][CH2:13][C:12]#[C:11][C:7]1[CH:6]=[C:5]([CH:10]=[CH:9][CH:8]=1)[C:4]([OH:21])=[O:3])=[O:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 112547173-(5-Dimethylcarbamoyl-pent-ynyl)benzoic acid ethyl ester

생성물 1

HCID 114823353-(5-Dimethylcarbamoyl-pent-1-ynyl)-benzoic acid수율 74%

실험 절차

3-(5-Dimethylcarbamoyl-pent-ynyl)benzoic acid ethyl ester (0.800 g, 2.78 mmol) was treated with sodium hydroxide 1M solution (6 mL) overnight. To the reaction mixture 7 mL of HCl 1M solution was added and the solvent was removed under vacuum. The residue was triturated with ethyl acetate, to give 3-(5-dimethylcarbamoyl-pent-1-ynyl)-benzoic acid (24) (0.590 g, 2.05 mmol; yield 74%) as white off powder.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • customthe solvent was removed under vacuum
  • customThe residue was triturated with ethyl acetate
  • 출처 및 근거

    ORD 기록
    ord-ed7009d4ab774e90be675bce89bf13f9
    출처 데이터셋
    uspto-grants-2012_10
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08293796B2

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