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Triazamate → Triazamate acid

HRID 1109243
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인쇄 미리보기

반응식

HRID 1109243 반응식
[CH3:1][N:2]([CH3:21])[C:3]([N:5]1[C:9]([S:10][CH2:11][C:12]([O:14]CC)=[O:13])=[N:8][C:7]([C:17]([CH3:20])([CH3:19])[CH3:18])=[N:6]1)=[O:4]>C1COCC1>[CH3:1][N:2]([CH3:21])[C:3]([N:5]1[C:9]([S:10][CH2:11][C:12]([OH:14])=[O:13])=[N:8][C:7]([C:17]([CH3:19])([CH3:18])[CH3:20])=[N:6]1)=[O:4]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 86306Triazamate

생성물 1

HCID 14299898Triazamate acid

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
20 °C

실험 절차

To 1.2 g of 1-dimethylearbamoyl-3-t-butyl-5-carboethoxyrmthylthio-1H-1,2,4-triazole (the compound of Example 2) in 20 ml of THF was added 4 ml of 12 M HC1. After stirring for 48 h at 20° C. the reaction mixture was partitioned between ether and water, the ether layer was extracted with dilute NAOH and the resulting aqueous layer was acidified and extracted with fresh ether. The resulting ether layer was dried over magnesium sulfate, filtered and evaporated under vacuum to yield 1-dimethylcarbamyl-3-t-butyl-5-carboxymethylthio-1H-1,2,4-triazole as an oil.

후처리

custom
was partitioned between ether and water
  • extractionthe ether layer was extracted with dilute NAOH
  • extractionextracted with fresh ether
  • dry with materialThe resulting ether layer was dried over magnesium sulfate
  • filtrationfiltered
  • customevaporated under vacuum
  • 출처 및 근거

    ORD 기록
    ord-cbcfb3988a2b48239a64a6262e0a47e3
    출처 데이터셋
    uspto-grants-1994_06
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05319092

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