2-(4-BENZYLPIPERAZINO)BENZALDEHYDE
- Product Name
- 2-(4-BENZYLPIPERAZINO)BENZALDEHYDE
- CAS No.
- 112253-26-6
- Chemical Name
- 2-(4-BENZYLPIPERAZINO)BENZALDEHYDE
- Synonyms
- 2-(4-BENZYLPIPERAZINO)BENZALDEHYDE;1-Benzyl-4-(2-formylphenyl)piperazine;2-(4-BENZYLPIPERAZIN-1-YL)BENZALDEHYDE;2-(4-BENZYLPIPERAZINO)BENZENECARBALDEHYDE;2-(4-BENZYLPIPERAZIN-1-YL)BENZALDEHYDE, 95+%;2-[4-(Phenylmethyl)-1-piperazinyl]benzaldehyde;Benzaldehyde, 2-[4-(phenylmethyl)-1-piperazinyl]-;2-[4-(phenylmethyl)-1-piperazin-4-iumyl]benzaldehyde;2-(4-BENZYLPIPERAZINO)BENZALDEHYDE ISO 9001:2015 REACH
- CBNumber
- CB5781094
- Molecular Formula
- C18H20N2O
- Formula Weight
- 280.36
- MOL File
- 112253-26-6.mol
2-(4-BENZYLPIPERAZINO)BENZALDEHYDE Property
- Melting point:
- 58 °C
- Boiling point:
- 429.9±45.0 °C(Predicted)
- Density
- 1.155±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- 7.46±0.10(Predicted)
- CAS DataBase Reference
- 112253-26-6(CAS DataBase Reference)
Safety
- Hazard Codes
- Xi
- HazardClass
- IRRITANT
- HS Code
- 2933599590
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- B289218
- Product name
- 2-(4-Benzylpiperazin-1-yl)benzaldehyde
- Packaging
- 10mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- OR29343
- Product name
- 2-(4-Benzylpiperazin-1-yl)benzaldehyde
- Packaging
- 1g
- Price
- $49
- Updated
- 2021/12/16
- Product number
- 4H15-1-W4
- Product name
- 2-(4-Benzylpiperazin-1-yl)benzaldehyde
- Packaging
- 1g
- Price
- $58
- Updated
- 2021/12/16
- Product number
- 046043
- Product name
- 2-(4-Benzylpiperazino)benzenecarbaldehyde
- Purity
- >95%
- Packaging
- 500mg
- Price
- $118
- Updated
- 2021/12/16
- Product number
- 046043
- Product name
- 2-(4-Benzylpiperazino)benzenecarbaldehyde
- Purity
- >95%
- Packaging
- 1g
- Price
- $151
- Updated
- 2021/12/16
2-(4-BENZYLPIPERAZINO)BENZALDEHYDE Chemical Properties,Usage,Production
Synthesis
2759-28-6
446-52-6
112253-26-6
Example 3: Synthesis of 1-[4-(1-methoxy-1-methyl-ethyl)-phenyl]-3-(2-piperazin-1-yl-benzo-D-pyrrolidin-2-one (Compound 12) Step 1: 25 g of 1-benzylpiperazine (1) and 10 g of 2-fluorobenzaldehyde (2) were reacted in refluxing dioxane/water (1:2, total volume 90 mL) in the presence of 17 g of K2CO3 for 24 hours. After completion of the reaction, the mixture was cooled to room temperature and extracted with dichloromethane. The organic layer was washed sequentially with water, 5% hydrochloric acid and brine, followed by drying with magnesium sulfate, filtration and concentration in vacuum. Purification by silica gel column chromatography (eluent: 5:1 hexane-ethyl acetate) afforded 20 g of 2-(4-benzylpiperazin-1-yl)benzaldehyde (3) in 89% yield; mass spectrum (AP/CI): m/z 281.1 ([M+H]+, 100%). Step 2: 8 g of 2-(4-benzylpiperazin-1-yl)benzaldehyde (3) was reacted with 4.6 g of NaH (60% mineral oil dispersion) at room temperature for 1 h. Subsequently, 7.3 g of 1-acetyl-pyrrolidin-2-one (4) was added, warmed up to room temperature and stirring was continued for 2 hours. The reaction solution was carefully quenched with methanol at 0°C and the solvent was removed in vacuum. The residue was diluted with water and extracted with dichloromethane. The organic layer was washed with brine, dried over magnesium sulfate, filtered and concentrated in vacuum. Purification by silica gel column chromatography (eluent: 40:1 chloroform-methanol) afforded 7.9 g of 3-[2-(4-benzylpiperazin-1-yl)-benzylidene]-pyrrolidin-2-one (5) in 80% yield; mass spectrum (AP/CI): m/z 348.1 ([M+H]+, 100%). Step 3: 6.3 g of 3-[2-(4-benzylpiperazin-1-yl)-benzylidene]-pyrrolidin-2-one (5) was catalytically hydrogenated with 1.5 g of Pd/C in 100 mL of methanol at 50 psi. Upon completion of the reaction, it was filtered and concentrated in vacuum to afford 3.8 g of 3-(2-piperazin-1-yl-benzylidene)-pyrrolidin-2-one (6) in 82% yield; purified by silica gel column chromatography (eluent: 30:1:0.3 chloroform-methanol-ammonium hydroxide); mass spectrum (AP/CI): m/z 260.1 ([M+H]+, 100%). Step 4: 1.2 g of 3-(2-piperazin-1-yl-benzyl)-pyrrolidin-2-one (6) was mixed with 0.041 g of N,N'-dimethylethylenediamine, 0.088 g of CuI, and 0.96 g of K2CO3 in 6 mL of toluene, and 1.27 g of 1-bromo-4-(1-methoxy-1-methyl- ethyl)-benzene (11) was added, and reacted for 17 h at 110 °C . After completion of the reaction, purification by silica gel column chromatography (eluent: 40:1:0.5 chloroform-methanol-ammonium hydroxide) afforded 1.2 g of the racemate 1-[4-(1-methoxy-1-methylethyl)-phenyl]-3-(2-piperazin-1-yl-benzyl)-pyrrolidin-2-one (12), in 64% yield; mass spectrum (AP/CI): m/z 408.2 ([M +H]+).
References
[1] Patent: WO2006/75226, 2006, A1. Location in patent: Page/Page column 23
[2] Synthesis, 1987, # 7, p. 641 - 645
2-(4-BENZYLPIPERAZINO)BENZALDEHYDE Preparation Products And Raw materials
Raw materials
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View Lastest Price from 2-(4-BENZYLPIPERAZINO)BENZALDEHYDE manufacturers
- Product
- 2-(4-BENZYLPIPERAZINO)BENZALDEHYDE 112253-26-6
- Price
- US $1.10/g
- Min. Order
- 1g
- Purity
- 99.00%
- Supply Ability
- 100 Tons
- Release date
- 2022-02-23
- Product
- 2-(4-BENZYLPIPERAZINO)BENZALDEHYDE 112253-26-6
- Price
- US $1.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- KG/T
- Release date
- 2019-12-19