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Allyl Alcohol → N-[3-(3-Oxo-propyl)-phenyl]-methanesulfonamide

HRID 15899
Notes
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Reaction equation

HRID 15899 reaction equation
I[C:2]1[CH:3]=[C:4]([NH:8][S:9]([CH3:12])(=[O:11])=[O:10])[CH:5]=[CH:6][CH:7]=1.[CH2:13]([OH:16])[CH:14]=[CH2:15].C(=O)([O-])O.[Na+]>[Cl-].C([N+](CCCC)(CCCC)CCCC)CCC.CN(C)C=O.Cl.[Pd](Cl)Cl>[O:16]=[CH:13][CH2:14][CH2:15][C:2]1[CH:3]=[C:4]([NH:8][S:9]([CH3:12])(=[O:11])=[O:10])[CH:5]=[CH:6][CH:7]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 3

HCID 7858Allyl AlcoholHCID 516892Sodium BicarbonateHCID 21830928N-(3-iodophenyl)methanesulfonamide

Product 1

HCID 57444373N-[3-(3-Oxo-propyl)-phenyl]-methanesulfonamideYield 60.5%

Reagents, catalysts & solvents 4

HCID 24290Palladium ChlorideCatalyst
HCID 70681
Tetrabutylammonium Chloride
Catalyst
HCID 313Hydrochloric AcidSolvent
HCID 6228DimethylformamideSolvent

Procedure

A mixture of N-(3-iodo-phenyl)-methanesulfonamide (2.4 g, 8 mmol), tetra-n-butyl-ammonium chloride (2.22 g, 8 mmol), allyl alcohol (0.7 g, 12 mmol), sodium hydrogencarbonate (1.6 g, 19 mmol) and palladium(II) chloride (0.36 g, 1.8 mmol) in anhydrous dimethylformamide (30 mL) was stirred at room temperature for 48 h under argon. The mixture was then diluted with 5% aqueous hydrochloric acid (100 mL) and extracted with ethyl acetate (2×100 mL). The combined organic layers were dried (sodium sulfate) and evaporated in vacuo. The crude product was purified by silica gel chromatography (ethyl acetate in hexane, 30% to 50%) to give the title compound as an amber oil (1.1 g, 60%).

Workup

  1. extractionextracted with ethyl acetate (2×100 mL)
  2. dry with materialThe combined organic layers were dried (sodium sulfate)
  3. customevaporated in vacuo
  4. customThe crude product was purified by silica gel chromatography (ethyl acetate in hexane, 30% to 50%)

Sources & evidence

ORD record
ord-c3abfdc781784af8ae3f38b4d5d92de5
Source dataset
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07732600B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes