Basic information Safety Supplier Related

4-METHYLPHTHALIMIDE 99

Basic information Safety Supplier Related

4-METHYLPHTHALIMIDE 99 Basic information

Product Name:
4-METHYLPHTHALIMIDE 99
Synonyms:
  • 5-methyl-1H-isoindole-1,3-(2H)-dione
  • 4-METHYLPHTHALIMIDE 99
  • 4-Methykphthalimide
  • 4-METHYLPHTHALIMIDE 96% C9H7NO2 FW161.16
  • 5-Methylisoindoline-1,3-dione
  • 5-Methyl-isoindole-1,3-dione
  • 1H-Isoindole-1,3(2H)-dione, 5-methyl-
CAS:
40314-06-5
MF:
C9H7NO2
MW:
161.16
Product Categories:
  • M
  • Stains and Dyes
  • Stains&Dyes, A to
  • Diels-Alder Adducts
Mol File:
40314-06-5.mol
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4-METHYLPHTHALIMIDE 99 Chemical Properties

Melting point:
196.5-199.5 °C(lit.)
Density 
1.301±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
10.09±0.20(Predicted)
form 
Solid
color 
Off-white to light brown
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Safety Information

WGK Germany 
3
HS Code 
2933998090
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4-METHYLPHTHALIMIDE 99 Usage And Synthesis

Uses

4-Methylphthalimide is a useful research chemical used in the preparation of imidobiaryls via ring opening reaction of cyclic diaryliodonium salts with imides by copper catalyst.

Synthesis

19438-61-0

40314-06-5

General procedure for the synthesis of 4-methylphthalimide from 5-methylisobenzofuran-1,3-dione (Intermediate Example 71): 5-methyl-2,3-dihydro-1H-isoindole xylene (15 mL) was added to a reaction vial containing 4-methylphthalic anhydride (3.0 g) and urea (1.2 g). The reaction mixture was stirred at 150°C overnight. After completion of the reaction, the mixture was cooled to room temperature and the precipitated crystals were collected by filtration and washed sequentially with ethanol and water. The resulting crystals were dried under reduced pressure to give 4-methylphthalimide (2.4 g, 82% yield) as white crystals.1H NMR (CDCl3) δ (ppm): 2.5 (3H, s), 7.5 (1H, d), 7.6 (1H, s), 7.7 (1H, s).

References

[1] Patent: EP1595866, 2005, A1. Location in patent: Page/Page column 27
[2] Bulletin of the Chemical Society of Japan, 2001, vol. 74, # 10, p. 1975 - 1976
[3] Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 14, p. 4159 - 4162
[4] Patent: EP1445249, 2004, A1. Location in patent: Page 133

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