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Dimethylformamide → HCID 54219924, 화합물

HRID 2198570
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인쇄 미리보기

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HRID 2198570 반응식
O([C:8]([C:10]1[CH:19]=[CH:18][C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[C:11]=1[OH:20])=[O:9])C1C=CC=CC=1.[S:21]([OH:31])(=[O:30])([C:23]1[CH:28]=[CH:27][C:26]([NH2:29])=[CH:25][CH:24]=1)=[O:22].C[N:33](C=O)C>C(N(CC)CC)C>[S:21]([C:23]1[CH:24]=[CH:25][C:26]([NH:29][NH:33][C:8]([C:10]2[CH:19]=[CH:18][C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:11]=2[OH:20])=[O:9])=[CH:27][CH:28]=1)([OH:31])(=[O:30])=[O:22]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 8479Sulfanilic acidHCID 67236Phenyl 1-hydroxy-2-naphthoate

생성물 1

HCID 54219924HCID 54219924, 화합물

시약·촉매·용매 1

HCID 8471Triethylamine용매

반응 조건

온도
170 °C

실험 절차

To 13.2 g of 2-phenoxycarbonyl-1-naphthol, 8.6 g of sulfanilic acid, 20 ml of DMF and 14 ml of triethylamine were added. The mixture was stirred at 170° C. for 5 hours. The mixture was concentrated at reduced pressure and methanol was added to the residue. The crystals thus-precipitated were collected by filtration.

후처리

  1. concentrationThe mixture was concentrated at reduced pressure and methanol
  2. additionwas added to the residue
  3. customThe crystals thus-precipitated
  4. filtrationwere collected by filtration

출처 및 근거

ORD 기록
ord-efbd86e8c1d24a2e93d32639a5a26f3a
출처 데이터셋
uspto-grants-1982_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04358526

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