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Hydrochloric Acid → 2-(4-Methoxybenzyl)-2h-tetrazole-5-carboxylic acid

HRID 325742
노트
인쇄 미리보기

반응식

HRID 325742 반응식
[CH3:1][O:2][C:3]1[CH:17]=[CH:16][C:6]([CH2:7][N:8]2[N:12]=[N:11][C:10]([C:13]([O-:15])=[O:14])=[N:9]2)=[CH:5][CH:4]=1.[K+].Cl>O>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:7][N:8]2[N:12]=[N:11][C:10]([C:13]([OH:15])=[O:14])=[N:9]2)=[CH:16][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 23677909potassium 2-(4-methoxybenzyl)-2H-tetrazole-5-carboxylate

생성물 1

HCID 135962442-(4-Methoxybenzyl)-2h-tetrazole-5-carboxylic acid수율 56.9%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Potassium 2-(4-methoxybenzyl)-2H-tetrazole-5-carboxylate (2.45 g) was dissolved in a minimum quantity of water and acidified to pH 1 by treatment with concentrated hydrochloric acid. The mixture was stirred for 3 hours, and then the solid was filtered off and washed with water to give 2-(4-methoxybenzyl)-2H-tetrazole-5-carboxylic acid (1.20 g), m.p. 146°-147° C. (with decomposition).

후처리

  1. filtrationthe solid was filtered off
  2. washwashed with water

출처 및 근거

ORD 기록
ord-92b9f2392cac41549c3f5f68dbc1dde4
출처 데이터셋
uspto-grants-1984_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04442115

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