Basic information Safety Supplier Related

FMOC-L-LEUCINOL

Basic information Safety Supplier Related

FMOC-L-LEUCINOL Basic information

Product Name:
FMOC-L-LEUCINOL
Synonyms:
  • Fmoc-L-Leu-OL
  • Fmoc-L-leucinol≥ 98% (HPLC)
  • Carbamic acid, N-[(1S)-1-(hydroxymethyl)-3-methylbutyl]-, 9H-fluoren-9-ylmethyl ester
  • N-(9-FLUORENYLMETHOXYCARBONYL)-L-LEUCINOL
  • N-ALPHA-FMOC-L-LEUCINOL
  • N-FMOC-L-LEUCINOL
  • (S)-(9H-fluoren-9-yl)methyl 1-hydroxy-4-methylpentan-2-ylcarbamate
  • REF DUPL: Fmoc-L-leucinol
CAS:
139551-83-0
MF:
C21H25NO3
MW:
339.43
Product Categories:
  • Amino Alcohols
  • Fmoc-Amino acid series
  • Amino Acids
Mol File:
139551-83-0.mol
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FMOC-L-LEUCINOL Chemical Properties

Melting point:
112-113 °C
Boiling point:
525.2±33.0 °C(Predicted)
Density 
1.148±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,2-8°C
pka
11.48±0.46(Predicted)
Appearance
White to off-white Solid
optical activity
-18.3°(C=0.01g/ml MEOH)
CAS DataBase Reference
139551-83-0(CAS DataBase Reference)
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FMOC-L-LEUCINOL Usage And Synthesis

Chemical Properties

White powder

Uses

Fmoc-L-leucinol is an intermediate used in the preparation of Fmoc-protected amino azides from Fmoc-protected amino alcohols.

Synthesis

35661-60-0

139551-83-0

GENERAL METHOD: To a tetrahydrofuran (THF, 10 mL) solution of Fmoc-L-leucine (10 mmol) was sequentially added N,N-diisopropylethylamine (DIPEA, 11 mmol, 1.42 mL) and 50% propylphosphonic anhydride (T3P) in ethyl acetate (EtOAc) solution (20 mmol, 6.36 mL) at 0 °C and the reaction mixture was stirred for about 10 min at this temperature. The reaction mixture was stirred for about 10 minutes. Subsequently, an aqueous solution of sodium borohydride (NaBH4, 10 mmol, 388 mg) (0.3 mL) was slowly added to the reaction system at the same temperature and the reaction was continuously stirred until the reaction was completed by thin layer chromatography (TLC). After completion of the reaction, the solvent was removed by rotary evaporator and the crude product was extracted with ethyl acetate (EtOAc). The organic phase was washed sequentially with 5% aqueous citric acid (10 mL × 2), 5% aqueous sodium carbonate (Na2CO3) (10 mL × 2), water and saturated saline. The organic layer was dried over anhydrous sodium sulfate (Na2SO4) and concentrated under reduced pressure to obtain Fmoc-L-leucinol.

References

[1] Journal of Organic Chemistry, 2001, vol. 66, # 25, p. 8454 - 8462
[2] Angewandte Chemie - International Edition, 2010, vol. 49, # 1, p. 117 - 120
[3] Organic and Biomolecular Chemistry, 2010, vol. 8, # 21, p. 4855 - 4860
[4] Tetrahedron Letters, 2012, vol. 53, # 38, p. 5059 - 5063
[5] Organic Letters, 2008, vol. 10, # 10, p. 1881 - 1884

FMOC-L-LEUCINOLSupplier

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