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Dimethylformamide → 3-Phenylbenzo[b]thiophene-2-carbaldehyde

HRID 1906757
Notes
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Reaction equation

HRID 1906757 reaction equation
C([Li])CCC.[C:6]1([C:12]2[C:13]3[CH:20]=[CH:19][CH:18]=[CH:17][C:14]=3[S:15][CH:16]=2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.CN(C)[CH:23]=[O:24]>O1CCCC1>[C:6]1([C:12]2[C:13]3[CH:20]=[CH:19][CH:18]=[CH:17][C:14]=3[S:15][C:16]=2[CH:23]=[O:24])[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 6228DimethylformamideHCID 6108813-PhenylbenzothiopheneHCID 178418339Butyllithium

Product 1

HCID 105141003-Phenylbenzo[b]thiophene-2-carbaldehyde

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Conditions

Temperature
-70 °C

Procedure

Butyllithium (62.5 ml of 1.6M solution in hexane, 0.1 mole) was added dropwise to a stirred solution of 3-phenylbenzo[b]thiophene (21.0 g, 0.1 mole) in tetrahydrofuran (150 ml) at -70° C. The solution was stirred at -70° C. for 30 minutes and dimethylformamide (10 ml, 0.13 mole) was added. The resulting mixture was stirred at -70° C. for 30 minutes and then allowed to warm to ambient temperature. After a further hour the reaction was quenched by the addition of dilute hydrochloric acid (100 ml, 2M) and the tetrahydrofuran removed under reduced pressure. The resulting oil was extracted into diethyl ether, the ethereal extract washed with water, dried over potassium carbonate and concentrated.

Workup

  1. stirringThe resulting mixture was stirred at -70° C. for 30 minutes
  2. temperatureto warm to ambient temperature
  3. customAfter a further hour the reaction was quenched by the addition of dilute hydrochloric acid (100 ml, 2M)
  4. customthe tetrahydrofuran removed under reduced pressure
  5. extractionThe resulting oil was extracted into diethyl ether
  6. extractionthe ethereal extract
  7. washwashed with water
  8. dry with materialdried over potassium carbonate
  9. concentrationconcentrated

Sources & evidence

ORD record
ord-6ab892673fc045028a5497921f9c43ee
Source dataset
uspto-grants-1987_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04654352

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes