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Hydrochloric Acid → 1-(4-Chlorobenzo[b]thiophen-2-yl)butan-1-one

HRID 2183643
Notes
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Reaction equation

HRID 2183643 reaction equation
[CH2:1]([Mg]Cl)[CH2:2][CH3:3].[Cl:6][C:7]1[C:15]2[CH:14]=[C:13]([C:16](N(OC)C)=[O:17])[S:12][C:11]=2[CH:10]=[CH:9][CH:8]=1.O.Cl>O1CCCC1>[Cl:6][C:7]1[C:15]2[CH:14]=[C:13]([C:16](=[O:17])[CH2:1][CH2:2][CH3:3])[S:12][C:11]=2[CH:10]=[CH:9][CH:8]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 962WaterHCID 224738924-chloro-N-methoxy-N-methylbenzo[b]thiophene-2-carboxamideHCID 178455855HCID 178455855, compound2×

Product 1

HCID 224736901-(4-Chlorobenzo[b]thiophen-2-yl)butan-1-one

Reagents, catalysts & solvents 1

HCID 8028
Tetrahydrofuran
Solvent

Procedure

Propylmagnesium chloride (2M solution in ether; 4.3 ml) was added under nitrogen over 15 minutes to a stirred solution of 4-chloro-N-methoxy-N-methylbenzo[b]thiophene-2-carboxamide (2 g) in tetrahydrofuran (25 ml) then the mixture was stirred at ambient temperature for 2.33 hours. Further propylmagnesium chloride (2M solution in ether; 0.5 ml) was added, the mixture was stirred at ambient temperature for 0.5 hours, then water (150 ml) and 5M hydrochloric acid (15 ml) were added. The product was extracted into dichloromethane (3×40 ml), the combined extracts were dried (MgSO4) and the solvents were removed in vacuo. The residue was purified by column chromatography over silica using dichloromethane as eluant. Appropriate fractions were combined and the solvents removed in vacuo to leave 1-(4-chlorobenzo[b]thiophen-2-yl)butan-1-one (0.95 g) which was used without further purification.

Workup

  1. stirringthe mixture was stirred at ambient temperature for 0.5 hours
  2. extractionThe product was extracted into dichloromethane (3×40 ml)
  3. dry with materialthe combined extracts were dried (MgSO4)
  4. customthe solvents were removed in vacuo
  5. customThe residue was purified by column chromatography over silica
  6. customthe solvents removed in vacuo

Sources & evidence

ORD record
ord-5cc97c0fdbce4ef689ec890feda21870
Source dataset
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06900216B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes