PHTHALIMIDOACETALDEHYDE DIETHYL ACETAL
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
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)
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
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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PHTHALIMIDOACETALDEHYDE DIETHYL ACETAL(78902-09-7)Related Product Information
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- ETHYL 3-O-BENZYL-4,6-O-BENZYLIDENE-2-DEOXY-2-PHTHALIMIDO-BETA-D-GLUCOPYRANOSIDE
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