2-Phthalimidoethanesulfonyl chloride

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2-Phthalimidoethanesulfonyl chloride manufacturers

2-Phthalimidoethanesulfonyl chloride Basic information
Product Name:2-Phthalimidoethanesulfonyl chloride
Synonyms:AKOS BBS-00004578;AKOS MSC-0752;2-(1,3-DIOXO-1,3-DIHYDRO-ISOINDOL-2-YL)-ETHANESULFONYL CHLORIDE;2-(1,3-Dioxo-2,3-dihydro-1H-isoindol-2-yl)ethane-1-sulfonyl chloride;2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-1-ethanesulfonyl chloride;2H-Isoindole-2-ethanesulfonyl chloride, 1,3-dihydro-1,3-dioxo-;2-Phthalimidoethanesulfonyl chlorid;2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethane-1-sulfonyl chloride
CAS:4403-36-5
MF:C10H8ClNO4S
MW:273.69
EINECS:610-161-4
Product Categories:Building Blocks;Chemical Synthesis;Organic Building Blocks;Sulfonyl Halides;Sulfur Compounds
Mol File:4403-36-5.mol
2-Phthalimidoethanesulfonyl chloride Structure
2-Phthalimidoethanesulfonyl chloride Chemical Properties
Melting point 158-163℃
Boiling point 416.5±28.0 °C(Predicted)
density 1.585±0.06 g/cm3(Predicted)
vapor pressure 0-0Pa at 20-50℃
storage temp. 2-8°C
pka-2.47±0.20(Predicted)
form Slurry
color Yellow to orange to brown
Water Solubility Reacts with water.
Sensitive Moisture Sensitive
Stability:Hygroscopic, Moisture Sensitive
InChI1S/C10H8ClNO4S/c11-17(15,16)6-5-12-9(13)7-3-1-2-4-8(7)10(12)14/h1-4H,5-6H2
InChIKeyHCPVYBCAYPMANM-UHFFFAOYSA-N
SMILESClS(=O)(=O)CCN1C(=O)c2ccccc2C1=O
LogP1.12-2.44 at 25℃
CAS DataBase Reference4403-36-5(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,C
Risk Statements 34
Safety Statements 26-36/37/39-45-60
RIDADR 3261
WGK Germany 3
HazardClass 8
PackingGroup II
HS Code 29251900
Storage Class11 - Combustible Solids
Hazard ClassificationsSkin Sens. 1
MSDS Information
ProviderLanguage
ALFA English
2-Phthalimidoethanesulfonyl chloride Usage And Synthesis
Uses2-(Phthalimido)ethanesulfonyl chloride is an important raw material and intermediate used in pharmaceuticals, agro based and dye stuff fields.
Synthesis
Phthalic anhydride

85-44-9

Taurine

107-35-7

2-PHTHALIMIDOETHANESULFONYL CHLORIDE

4403-36-5

The general procedure for the synthesis of 2-phenylenedi(meth)iminoethane sulfonyl chloride from phthalic anhydride and taurine is as follows:1. A suspension of taurine (8.0 g, 63.9 mmol) and potassium acetate (6.7 g, 68.3 mmol) was refluxed in acetic acid for 15 min. 2. Phthalic anhydride (10.1 g, 68.4 mmol) was added, and the reaction was continued to be refluxed for 3 h. 3. Upon completion of the reaction, the reaction was cooled to room temperature, the solid product was collected by filtration, washed with cold acetic acid and dried under vacuum at 100 °C to give a white solid.4. The above white solid (14.3 g, 54.7 mmol) was suspended in toluene (50 ml), and phosphorus pentachloride (8.12 g, 39.0 mmol) was added under the protection of nitrogen.5. After the reaction mixture was heated and refluxed for 1 hour The reaction mixture was heated and refluxed for 1 hour, then phosphorus pentachloride (8.12 g, 39.0 mmol) was added again and refluxing was continued for another 2.5 hours.6 Upon completion of the reaction, a brownish solution was poured from a small amount of the solid formed, and the solution was subsequently concentrated under vacuum.7 The concentrated residue was poured into a mixture of ice and water (ice:water=50:50, 100 ml), and the solid product was filtered to collect the solid product.8 Finally, the solid was dried under vacuum at 45°C for 16 hours to obtain a light brown color.9 The reaction was carried out under nitrogen protection. Vacuum dried for 16 hours to give a light brown solid product (6.4 g, 34% yield).

References[1] Patent: US6313312, 2001, B1
[2] Archiv der Pharmazie, 2007, vol. 340, # 12, p. 656 - 660
[3] Journal of Medicinal Chemistry, 2010, vol. 53, # 6, p. 2390 - 2400
[4] European Journal of Medicinal Chemistry, 2018, vol. 146, p. 108 - 122
Tag:2-Phthalimidoethanesulfonyl chloride(4403-36-5) Related Product Information
2-Phthalimidoethanesulfonyl chloride Ethanesulfonyl chloride Ethanethiol, 2-phthalimido- Nsc190757 N,N-phthaloyl-taurine 1H-Isoindole-1,3(2H)-dione, 2-[2-[(trifluoromethyl)sulfonyl]ethyl]-