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85185-24-6

85185-24-6 Structure

85185-24-6 Structure
IdentificationBack Directory
[Name]

3-(N-Boc)pentanedioic acid
[CAS]

85185-24-6
[Synonyms]

3-(N-Boc)pentanedioic acid
N-Boc-3-aminopentanedioic acid
3-tert-butoxycarbonylaminopentanedioic acid
Pentanedioic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-
3-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)pentanedioic acid
[Molecular Formula]

C10H17NO6
[MDL Number]

MFCD14705046
[MOL File]

85185-24-6.mol
[Molecular Weight]

247.25
Chemical PropertiesBack Directory
[Boiling point ]

429.8±35.0 °C(Predicted)
[density ]

1.264±0.06 g/cm3(Predicted)
[pka]

4.00±0.10(Predicted)
Hazard InformationBack Directory
[Synthesis]

3-AMINOPENTANEDIOIC ACID

1948-48-7

Di-tert-butyl dicarbonate

24424-99-5

3-(N-Boc)pentanedioic acid

85185-24-6

General procedure for the synthesis of 3-((tert-butoxycarbonyl)amino)glutaric acid from β-glutamic acid and di-tert-butyl dicarbonate: β-glutamic acid (1.01 g, 6.8 mmol) was dissolved in a mixed solvent of tetrahydrofuran (30 mL) and water (15 mL). Subsequently, di-tert-butyl dicarbonate (2.98 g, 13.6 mmol) and 10% aqueous sodium hydroxide (8.3 mL) were added and the reaction mixture was stirred at room temperature for 5 days. Upon completion of the reaction, the solvent was removed by evaporation and the residue was redissolved in water (30 mL) and the pH was adjusted to 2 with 1 M potassium bisulfate solution. the aqueous phase was extracted with ethyl acetate (2 x 60 mL), the organic layers were combined, dried with anhydrous sodium sulfate, filtered and concentrated to afford 1.5 g (90% yield) of 3-((tert-butoxycarbonyl)amino)glutaric acid as a white crystal. The product was confirmed by NMR hydrogen spectroscopy (MeOD): δ 1.43 (s, 9H), 2.55 (d, 4H), 4.25 (quin, 1H). HPLC-MS (Method B) showed: m/z 148 ([M+1-Boc]+).

[References]

[1] Patent: WO2004/89362, 2004, A1. Location in patent: Page/Page column 64
[2] Asian Journal of Chemistry, 2014, vol. 26, # 15, p. 4716 - 4722
[3] Chemistry Letters, 1988, # 10, p. 1643 - 1646
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