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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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3-[(1H-Indol-3-yl)sulfanyl]prop-2-enoic acid → Thiopyrano[3,2-b]indol-4(5H)-one

HRID 372758
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HRID 372758 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([S:10][CH:11]=[CH:12][C:13]([OH:15])=O)=[CH:2]1>C(O)(=O)C>[S:10]1[C:3]2[C:4]3[CH:5]=[CH:6][CH:7]=[CH:8][C:9]=3[NH:1][C:2]=2[C:13](=[O:15])[CH:12]=[CH:11]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 544439283-[(1H-Indol-3-yl)sulfanyl]prop-2-enoic acid

생성물 1

HCID 20326608Thiopyrano[3,2-b]indol-4(5H)-one수율 53.7%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

-- A solution of 76.7 g (0.35 mole) of 3-(indol-3 ylthio) acrylic acid in 4 liters of 10% polyphosphoric acid in acetic acid is stirred at room temperature for 65 hours. The supernatent is decanted from the sticky precipitate, which is partitioned between chloroform and 5% NaOH solution. The organic phase is washed with water, dried, evaporated and the residue recrystallized from 3 liters of 95% ethanol to give 37.8 g of product, mp 242°-243° C.

후처리

  1. customThe supernatent is decanted from the sticky precipitate, which
  2. customis partitioned between chloroform and 5% NaOH solution
  3. washThe organic phase is washed with water
  4. customdried
  5. customevaporated
  6. customthe residue recrystallized from 3 liters of 95% ethanol

출처 및 근거

ORD 기록
ord-a25ff836b72940b6a870c95dcc31b791
출처 데이터셋
uspto-grants-1978_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04092328

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