Dichloromethane → 3-[3-(Naphthalen-2-ylsulfamoyl)phenyl]-acryloyl Chloride

HRID 2180412Notes

Reaction equation

HRID 2180412 reaction equation
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[NH:11][S:12]([C:15]1[CH:16]=[C:17]([CH:21]=[CH:22][C:23]([OH:25])=O)[CH:18]=[CH:19][CH:20]=1)(=[O:14])=[O:13].[Cl:26]CCl>CN(C)C=O>[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[NH:11][S:12]([C:15]1[CH:16]=[C:17]([CH:21]=[CH:22][C:23]([Cl:26])=[O:25])[CH:18]=[CH:19][CH:20]=1)(=[O:14])=[O:13]

Participants

4

Reactant 2

HCID 6344DichloromethaneHCID 670195903-[3-(Naphthalen-2-ylsulfamoyl)-phenyl]-acrylic acid

Product 1

HCID 739894303-[3-(Naphthalen-2-ylsulfamoyl)phenyl]-acryloyl ChlorideYield 99.1%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideCatalyst

Conditions

Temperature
40 °C

Procedure

To a suspension of 3-[3-(naphthalen-2-ylsulfamoyl)-phenyl]-acrylic acid (15e) (0.21 g, 0.57 mmol) in dichloromethane (2.5 ml) oxalyl chloride (0.15 ml, 1.71 mmol) and one drop of dimethylformamide were added. The reaction mixture was stirred at 40° C. for one hour and concentrated under reduced pressure to give crude title compound (0.21 g, 95%).

Workup

  1. additionwere added
  2. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-8d1b697fb2d842e59ef185b23e4eba85
Source dataset
uspto-grants-2005_05
Patent number
US06888027B2

Reaction notes

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