N-1-Boc-amino-3-cyclopentene Chemical Properties

Boiling point:

268.9±20.0 °C(Predicted)

Density 

1.01±0.1 g/cm3(Predicted)

storage temp. 

2-8°C

pka

12.37±0.20(Predicted)

form 

solid

color 

Yellow

CAS DataBase Reference

193751-54-1(CAS DataBase Reference)

Safety Information

Risk Statements 

36/37/38

Safety Statements 

26-36/37/39

HS Code 

2924297099

N-1-Boc-amino-3-cyclopentene Usage And Synthesis

Uses

N-1-Boc-amino-3-cyclopentene is a cyclopentenamine with a protecting group used to explore the feasibility of using small molecules to functionalize Si surfaces with primary amine groups for DNA attachment.

Synthesis

GENERAL STEPS: To a three-necked round-bottomed flask cooled in an ice-water bath was added an anhydrous tetrahydrofuran (THF, 10 mL) solution of triphenylphosphine (Ph3P, 0.015 mol), followed by an anhydrous THF (10 mL) solution of 3-cyclopenten-1-ol (II, 0.012 mol) and an anhydrous THF (0.015 mol) solution of N-Boc-ethyl oxalate ( 10 mL) solution. Diethyl azodicarboxylate (DEAD, 0.015 mol) was slowly added dropwise to the above mixture. The reaction mixture was stirred at 0°C for 2 hours, followed by continuing the reaction at room temperature for 48 hours. Upon completion of the reaction, the solvent was removed by reduced pressure distillation and the residue was dissolved in dichloromethane (CH2Cl2, 30 mL) and washed sequentially with water and brine (20 mL x 3). The solvent was again removed by reduced pressure distillation and the residue was purified by column chromatography (silica gel, 100% dichloromethane) to afford a mixture of ethyl (tert-butoxycarbonyl-cyclopent-3-enyl-amino)-oxo-acetate and N-Boc-ethylcarbamate, which was used for the next reaction without further purification. The above crude product (3.80 g) was dissolved in THF (35 mL), cooled in an ice-water bath and stirred, and a solution of lithium hydroxide (LiOH, 0.0765 mol) in water (35 mL) was slowly added. The mixture was continued to be stirred in an ice-water bath for 3 hours. Upon completion of the reaction, the organic material was extracted with dichloromethane (30 mL x 3), the organic layers were combined and washed with brine (30 mL x 2), and the solvent was subsequently removed by distillation under reduced pressure. The residue was purified by column chromatography (silica gel, 100% dichloromethane) to give white crystals of the pure product in 53% yield.

References

[1] Patent: WO2005/26111, 2005, A2. Location in patent: Page/Page column 20
[2] Patent: WO2008/42353, 2008, A1. Location in patent: Page/Page column 24
[3] Patent: WO2008/42353, 2008, A1. Location in patent: Page/Page column 24

N-1-Boc-amino-3-cyclopentene(193751-54-1)Related Product Information

• Cyhalofop-butyl
• Dibutyl phthalate
• Diethylene glycol monobutyl ether
• Butyl acetate
• EC 2.6.1.2
• BUTYL OLEATE
• ALTRENOGEST
• Buprofezin
• N-Carbobenzyloxyglycine
• Methyl cyclopentenolone
• Acetaminophen
• 6-Aminocaproic acid
• Glucosamine
• Sulfamic acid
• 3-Aminophenol
• tert-Butyl carbazate
• Glycine
• Tris(hydroxymethyl)aminomethane