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Hydrochloric Acid → HCID 178427247, 화합물

HRID 614827
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HRID 614827 반응식
FC(F)(F)C(O)=O.N1C(C)=CC=CC=1C.[C:16]([C:18]1[CH:26]=[C:25]([CH3:27])[CH:24]=[C:20]([C:21]([OH:23])=[O:22])[C:19]=1[OH:28])#[N:17].[N-:29]=[N+:30]=[N-:31].[Na+].[Cl-].[Li+].Cl>O>[CH3:27][C:25]1[CH:24]=[C:20]([C:21]([OH:23])=[O:22])[C:19]([OH:28])=[C:18]([C:16]2[NH:31][N:30]=[N:29][N:17]=2)[CH:26]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 6

HCID 313Hydrochloric AcidHCID 6422Trifluoroacetic acidHCID 79372,6-LutidineHCID 33557Sodium AzideHCID 433294Lithium ChlorideHCID 130269333-Cyano-2-hydroxy-5-methylbenzoic acid

생성물 1

HCID 178427247HCID 178427247, 화합물
수율 59.1%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

Trifluoroacetic acid (0.8 ml) was added to dry 2,6-lutidine (10 ml) and the mixture was then treated with 3-cyano-5-methylsalicylic acid (0.885 g), sodium azide (0.65 g) and lithium chloride (20 mg), and heated at reflux for 20 hours. The mixture was then diluted with water (20 ml) and acidified by treatment with concentrated hydrochloric acid. The resulting precipitate was collected and recrystallized from a large amount of acetic acid to give 5-methyl-3-(tetrazol-5-yl)salicylic acid (0.65 g), m.p. 290°-292° C. (with decomposition).

후처리

  1. temperatureheated
  2. temperatureat reflux for 20 hours
  3. customThe resulting precipitate was collected
  4. customrecrystallized from a large amount of acetic acid

출처 및 근거

ORD 기록
ord-8086c434d1574442bcc5d4a5a726eeed
출처 데이터셋
uspto-grants-1979_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04146631

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