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Toluene → Ethyl 2-chloro-5-sulfamoylthiophene-3-carboxylate

HRID 1197427
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HRID 1197427 반응식
[Cl:1][C:2]1[S:6][C:5]([S:7]([NH2:10])(=[O:9])=[O:8])=[CH:4][C:3]=1[C:11]([OH:13])=[O:12].[C:14]1(C)C=CC=C[CH:15]=1>OS(O)(=O)=O.C(O)C>[Cl:1][C:2]1[S:6][C:5]([S:7]([NH2:10])(=[O:9])=[O:8])=[CH:4][C:3]=1[C:11]([O:13][CH2:14][CH3:15])=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 1140TolueneHCID 12014982-Chloro-5-sulfamoylthiophene-3-carboxylic acid

생성물 1

HCID 19106450Ethyl 2-chloro-5-sulfamoylthiophene-3-carboxylate

시약·촉매·용매 2

HCID 1118Sulfuric Acid촉매HCID 702Ethanol용매

실험 절차

To a round bottom flask were added 5-chloro-4-carboxythiophene-2-sulfonamide (5.0 g, 20.7 mmole) along with toluene (25 mL), ethanol (20 ml), and conc. H2SO4 (25 drops). The reaction mixture was refluxed for 96 hours. The reaction mixture was cooled and the solvent was removed under vacuum. The residue was then poured onto ice and the pH adjusted to ~8.0 using 10% sodium carbonate. The basic aqueous layer was extracted with ethyl acetate and the organic layer was washed with water, brine, and dried (MgSO4). Solvent removal yielded 3.92 g (70%) of an off white solid which was used as is: mp =98°-99° C.

후처리

  1. temperatureThe reaction mixture was refluxed for 96 hours
  2. temperatureThe reaction mixture was cooled
  3. customthe solvent was removed under vacuum
  4. additionThe residue was then poured onto ice
  5. extractionThe basic aqueous layer was extracted with ethyl acetate
  6. washthe organic layer was washed with water, brine
  7. dry with materialdried (MgSO4)
  8. customSolvent removal
  9. customyielded 3.92 g (70%) of an off white solid which
  10. custommp =98°-99° C.

출처 및 근거

ORD 기록
ord-8077273d383c4c3991829319258dbb7d
출처 데이터셋
uspto-grants-1994_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05276025

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