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Methane → Dazoxiben Hydrochloride

HRID 1462929
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인쇄 미리보기

반응식

HRID 1462929 반응식
[I-].C([N+:5]1[CH:9]=[CH:8][N:7]([CH2:10][CH2:11][O:12][C:13]2[CH:18]=[CH:17][C:16]([C:19]([O:21]CC)=[O:20])=[CH:15][CH:14]=2)[CH:6]=1)(=O)C.[ClH:24].C>>[ClH:24].[N:7]1([CH2:10][CH2:11][O:12][C:13]2[CH:18]=[CH:17][C:16]([C:19]([OH:21])=[O:20])=[CH:15][CH:14]=2)[CH:8]=[CH:9][N:5]=[CH:6]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 297MethaneHCID 313Hydrochloric AcidHCID 178469086HCID 178469086, 화합물

생성물 1

HCID 53000Dazoxiben Hydrochloride수율 79%

반응 조건

온도
80 °C

실험 절차

A mixture of 1.3 g of 1-acetyl-3-[2-(4-ethoxycarbonylphenoxy)ethyl]imidazolium iodide in 100 ml of 2N-hydrochloric acid was heated at 80° C. for 2 hours. After cooling, the solution was treated with an activated charcoal and concentrated under reduced pressure. The residue were triturated with acetone and the resulting crystals were filtered and dried to obtain 0.64 g of 4-[2-(1-imidazolyl)ethoxy]benzoic acid hydrochloride (79.0% yield). Colorless granules.

후처리

  1. temperatureAfter cooling
  2. concentrationconcentrated under reduced pressure
  3. customThe residue were triturated with acetone
  4. filtrationthe resulting crystals were filtered
  5. customdried

출처 및 근거

ORD 기록
ord-5689bed42282430796536df83ba3995b
출처 데이터셋
uspto-grants-1984_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04461905

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