Basic information Safety Supplier Related

PHTHALIMIDOACETALDEHYDE DIETHYL ACETAL

Basic information Safety Supplier Related

PHTHALIMIDOACETALDEHYDE DIETHYL ACETAL Basic information

Product Name:
PHTHALIMIDOACETALDEHYDE DIETHYL ACETAL
Synonyms:
  • LABOTEST-BB LT00454122
  • 2-PHTHALIMIDOACETALDEHYDE DIETHYL ACETAL
  • PHTHALIMIDOACETALDEHYDE DIETHYL ACETAL
  • N-(2,2-DIETHOXYETHYL)PHTHALIMIDE
  • 2-(Phthalimido)acetaldehyde diethylacetal 98%
  • phthalimido-acetaldehyde hydrate
  • 2-Phthalimidylacetaldehyde diethyl acetal
  • Phthalimidoacetaldehyde diethyl acetal,98+%
CAS:
78902-09-7
MF:
C14H17NO4
MW:
263.29
Product Categories:
  • N-Substituted Maleimides, Succinimides & Phthalimides
  • N-Substituted Phthalimides
Mol File:
78902-09-7.mol
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PHTHALIMIDOACETALDEHYDE DIETHYL ACETAL Chemical Properties

Melting point:
72-74 °C (lit.)
Boiling point:
372.3±32.0 °C(Predicted)
Density 
1.200±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
-2.17±0.20(Predicted)
form 
powder to crystal
color 
Light yellow to Yellow to Orange
Water Solubility 
Insoluble in water.
Sensitive 
Moisture Sensitive
BRN 
215793
CAS DataBase Reference
78902-09-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29126000

MSDS

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PHTHALIMIDOACETALDEHYDE DIETHYL ACETAL Usage And Synthesis

Chemical Properties

off-white to white powder

Uses

Phthalimidoacetaldehyde diethyl acetal is used as a pharmaceutical intermediate.

Synthesis

1074-82-4

2032-35-1

78902-09-7

The general procedure for the synthesis of benzoyliminoacetaldehyde diethyl acetal from potassium phthalimide salt and bromoacetaldehyde diethyl acetal was as follows: potassium phthalimide (5 g, 26.5 mmol), bromoacetaldehyde diethyl acetal (4.1 mL, 26.5 mmol), and cetyltributylphosphonium bromide (13.8 g, 26.5 mmol) were reacted under nitrogen protection in toluene ( 200 mL) at 111°C for 24 hours under nitrogen protection. After completion of the reaction, the mixture was filtered and the filtrate was concentrated by rotary evaporation to give a yellow oil. The target compound was purified by column chromatography (eluent: hexane/ether=1:1). The yield was 70%. Elemental analysis results (calculated value C14H17NO4, 263.29): C 63.8, H 6.4, N 5.3; measured value: C 64.6, H 6.5, N 5.3. 1H NMR (300MHz, CDCl3): δ7.8-7.6 (m, 4H), 4.79 (t, 1H), 3.75 (d, 2H), 3.62-3.42 (m, 4H), 1.06 (t, 6H).ES-MS: m/z 264.IR: ν(C-O-C) 2800, (C=O) 1721 cm-1.

References

[1] Russian Journal of General Chemistry, 2007, vol. 77, # 1, p. 98 - 102
[2] Journal of Chemistry, 2015, vol. 2015,
[3] Patent: WO2017/32840, 2017, A1. Location in patent: Page/Page column 264; 265
[4] Journal of Pharmacy and Pharmacology, 1952, vol. 4, p. 693,705

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