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

HRID 1860249
Notes
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Reaction equation

HRID 1860249 reaction equation
[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
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

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].

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  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

Sources & evidence

ORD record
ord-e19d464d563141de9198fd02aa0368cd
Source dataset
uspto-grants-2003_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06528653B2

Reaction notes

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