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Trimethylaluminum → 4,6-Dihydrothieno[2,3-b]pyrrol-5-one

HRID 1860249
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HRID 1860249 반응식
[NH2:1][C:2]1[S:3][CH:4]=[CH:5][C:6]=1[CH2:7][C:8]([O:10]CC)=O.C[Al](C)C>O1CCCC1>[S:3]1[C:2]2[NH:1][C:8](=[O:10])[CH2:7][C:6]=2[CH:5]=[CH:4]1
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참가 물질

4

반응물 2

HCID 16682925TrimethylaluminumHCID 53656999Ethyl 2-aminothiophene-3-acetate

생성물 1

HCID 113555184,6-Dihydrothieno[2,3-b]pyrrol-5-one수율 59.9%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Ethyl 2-aminothiophene-3-acetate (100 mg, 0.54 mmol) was dissolved in dry tetrahydrofuran (5 ml) and treated at −78° C. with trimethylaluminium (2M in n-heptane, 0.59 mmol). The reaction mixture was allowed to warm slowly to room temperature over 4 hours, cooled to 0° C. and quenched with saturated aqueous ammonium chloride solution. The solution was extracted with ethyl acetate and the organic phase dried over magnesium sulfate, evaporated to dryness and the residue chromatographed on silica gel using hexane/ethyl acetate (2:1) as eluent to give 45 mg of 4,6-dihydrothieno[2,3-b]pyrrol-5-one as a brown solid. MS(ES): m/e 140 [M+H].

후처리

  1. temperaturecooled to 0° C.
  2. customquenched with saturated aqueous ammonium chloride solution
  3. extractionThe solution was extracted with ethyl acetate
  4. dry with materialthe organic phase dried over magnesium sulfate
  5. customevaporated to dryness
  6. customthe residue chromatographed on silica gel

출처 및 근거

ORD 기록
ord-e19d464d563141de9198fd02aa0368cd
출처 데이터셋
uspto-grants-2003_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06528653B2

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