Dimethyl Sulfoxide → 4-(2-Benzoyl-4-chlorophenyl)-1H-pyrrole-3-carbonitrile

HRID 1995522Notes

Reaction equation

HRID 1995522 reaction equation
[C:1]([C:9]1[CH:14]=[C:13]([Cl:15])[CH:12]=[CH:11][C:10]=1[CH:16]=[CH:17][C:18]#[N:19])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S([CH2:30][N+:31]#[C-])(C1C=CC(C)=CC=1)(=O)=O.[CH3:33]S(C)=O.[H-].[Na+]>O.CCOCC>[C:1]([C:9]1[CH:14]=[C:13]([Cl:15])[CH:12]=[CH:11][C:10]=1[C:16]1[C:17]([C:30]#[N:31])=[CH:18][NH:19][CH:33]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

7

Reactant 4

HCID 679Dimethyl SulfoxideHCID 24758Sodium hydrideHCID 161915Tosylmethyl isocyanideHCID 543140203-(2-Benzoyl-4-chlorophenyl)prop-2-enenitrile

Product 1

HCID 130670864-(2-Benzoyl-4-chlorophenyl)-1H-pyrrole-3-carbonitrile

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 3283Diethyl EtherSolvent2×

Procedure

A mixture of 10.7 g (40 mmole) of 3-(2-benzoyl-4-chlorophenyl)-2-propenenitrile, 5.3 g (38 mmole) of tosylmethyl isocyanide, 75 ml of dimethyl sulfoxide and 150 of ether was added dropwise to a suspension of 3.7 g (77 mmole) of 50% sodium hydride in mineral oil and 170 ml of ether. When the addition was complete stirring was continued for 2 hr. The mixture was diluted with water and the ether layer was separated. The aqueous solution was extracted with ether. The combined ether extracts were washed with water, dried over anhydrous sodium sulfate; and concentrated at reduced pressure to give a dark green oil. Purification by column chromatography (800 g silica gel; eluent 5% ether in methylene chloride) gave end product as off-white prisms, mp 175°-177°.

Workup

  1. additionWhen the addition
  2. customthe ether layer was separated
  3. extractionThe aqueous solution was extracted with ether
  4. washThe combined ether extracts were washed with water
  5. dry with materialdried over anhydrous sodium sulfate
  6. concentrationand concentrated at reduced pressure
  7. customto give a dark green oil
  8. customPurification by column chromatography (800 g silica gel; eluent 5% ether in methylene chloride)
  9. customgave end product as off-white prisms, mp 175°-177°

Sources & evidence

ORD record
ord-9dd8251f990e4209a4ea5c13c742a46c
Source dataset
uspto-grants-1983_09
Patent number
US04405518

Reaction notes

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