Basic information Safety Supplier Related

(R)-2-N-CBZ-AMINO-PENTANE-1,5-DIOL

Basic information Safety Supplier Related

(R)-2-N-CBZ-AMINO-PENTANE-1,5-DIOL Basic information

Product Name:
(R)-2-N-CBZ-AMINO-PENTANE-1,5-DIOL
Synonyms:
  • (R)-Benzyl 1,5-dihydroxypentan-2-ylcarbamate
  • (R)-2-N-Cbz-aminopentane-1,5-diol
  • (R)-(4-Hydroxy-1-hydroxymethylbutyl)carbamic acid benzyl ester
  • REF DUPL: (R)-2-N-Cbz-amino-pentane-1,5-diol
  • REF DUPL: (S)-benzyl 1,5-dihydroxypentan-2-ylcarbamate
  • Carbamic acid, [(1R)-4-hydroxy-1-(hydroxymethyl)butyl]-, phenylmethyl ester (9CI)
  • Carbamic acid, N-[(1R)-4-hydroxy-1-(hydroxymethyl)butyl]-, phenylmethyl ester
  • benzyl (R)-(1,5-dihydroxypentan-2-yl)carbamate
CAS:
478646-28-5
MF:
C13H19NO4
MW:
253.29
Mol File:
478646-28-5.mol
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(R)-2-N-CBZ-AMINO-PENTANE-1,5-DIOL Chemical Properties

Boiling point:
485.2±45.0 °C(Predicted)
Density 
1.192±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
11.77±0.46(Predicted)
Appearance
White to off-white Solid
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(R)-2-N-CBZ-AMINO-PENTANE-1,5-DIOL Usage And Synthesis

Synthesis

67436-17-3

478646-28-5

General procedure: In a dry four-necked flask equipped with a dropping funnel and thermometer, 150 g of (S)-dimethyl 2-(((benzyloxy)carbonyl)amino)pentanediyl ester (η= 2) was added. After cooling the reaction system to 0-10 °C, 150 g of tetrahydrofuran was added to dissolve the feedstock. Subsequently, 29 g of sodium borohydride was slowly added and 72 g of anhydrous ethanol was added. The reaction was carried out at 10~15°C and terminated by dropwise addition of 90 g of acetic acid. The pH of the reaction solution was adjusted to 4~5 and extracted by adding 330 g of water and 350 g of ethyl acetate. The organic phase was separated, washed sequentially with sodium carbonate solution and saturated brine, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure (-0.1 MPa, temperature below 45 °C) to give a solid product. Beating with 102 g of n-heptane, filtration and drying gave 111.5 g of (R)-2-N-Cbz-aminopentane-1,5-diol (compound of formula IV) as a white solid. The yield was 90.8%, chemical purity 96.3% and optical purity 99.8%.

References

[1] Patent: CN103570601, 2016, B. Location in patent: Paragraph 0066; 0067

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