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Hydrochloric Acid → HCID 178435618, 화합물

HRID 867192
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HRID 867192 반응식
[C:1]([C:3]1[CH:4]=[CH:5][C:6]2[C:7](=[O:19])[C:8]3[C:13]([S:14][C:15]=2[CH:16]=1)=[CH:12][CH:11]=[C:10]([CH2:17][CH3:18])[CH:9]=3)#[N:2].[N-:20]=[N+:21]=[N-:22].[Na+].[Cl-].[NH4+].Cl>CN(C)C=O>[CH2:17]([C:10]1[CH:9]=[C:8]2[C:13]([S:14][C:15]3[CH:16]=[C:3]([C:1]4[NH:22][N:21]=[N:20][N:2]=4)[CH:4]=[CH:5][C:6]=3[C:7]2=[O:19])=[CH:12][CH:11]=1)[CH3:18]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 25517Ammonium ChlorideHCID 33557Sodium AzideHCID 10563642HCID 10563642, 화합물

생성물 1

HCID 178435618HCID 178435618, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

3-Cyano-7-ethylthioxanthone (5.3 g), sodium azide (1.55 g), and ammonium chloride (1.26 g) in dimethylformamide were heated at 120° C. for 3 hours, cooled, and poured into dilute hydrochloric acid. The solid precipitate was filtered off and recrystallised twice from acetic acid to yield 7-ethyl-3-(5-tetrazolyl)thioxanthone m.p. 247° C. with decomposition.

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후처리

  1. temperaturecooled
  2. filtrationThe solid precipitate was filtered off
  3. customrecrystallised twice from acetic acid

출처 및 근거

ORD 기록
ord-27ba1eff69cf46f5ab1b3db91cc73e23
출처 데이터셋
uspto-grants-1978_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04103015

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