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Hydrochloric Acid → 3-(4-isopropoxyphenyl)-1H-pyrazole-4-carbaldehyde hydrochloride

HRID 526769
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인쇄 미리보기

반응식

HRID 526769 반응식
[CH:1]([O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[C:15]([CH:16]=[O:17])=[CH:14][N:13](C3CCCCO3)[N:12]=2)=[CH:7][CH:6]=1)([CH3:3])[CH3:2].[ClH:24]>>[ClH:24].[CH:1]([O:4][C:5]1[CH:10]=[CH:9][C:8]([C:11]2[C:15]([CH:16]=[O:17])=[CH:14][NH:13][N:12]=2)=[CH:7][CH:6]=1)([CH3:3])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 313Hydrochloric AcidHCID 1176662103-(4-Isopropoxy-phenyl)-1-(tetrahydro-pyran-2-yl)-1H-pyrazole-4-carbaldehyde

생성물 1

HCID 1784582693-(4-isopropoxyphenyl)-1H-pyrazole-4-carbaldehyde hydrochloride수율 98%

실험 절차

A solution of 3-(4-isopropoxyphenyl)-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole-4-carbaldehyde (7.4 g, 23.56 mmol) in 3M methanolic HCl (74 mL) was stirred at rt for 3 h. The resulting solution was concentrated and triturated using diethyl ether (50 mL×3) to afford 3-(4-isopropoxyphenyl)-1H-pyrazole-4-carbaldehyde hydrochloride (5.3 g, yield 98%). LCMS (method C): RT=1.96 min, m/z=231.1 [M+H]+.

후처리

  1. concentrationThe resulting solution was concentrated
  2. customtriturated

출처 및 근거

ORD 기록
ord-0aea8fd604964b55b591db98cba9c097
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09346761B2

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