Basic information Safety Supplier Related

BOC-TRP-OBZL

Basic information Safety Supplier Related

BOC-TRP-OBZL Basic information

Product Name:
BOC-TRP-OBZL
Synonyms:
  • BOC-TRP-OBZL
  • BOC-L-TRYPTOPHAN BENZYL ESTER
  • N-α-Boc-L-Tryptophan benzyl ester
  • N-a-Boc-L-Tryptophanbenzylester
  • N-.ALPHA.-BOC-L-TRYPTOPHAN BENZYL ESTER
  • (S)-benzyl 2-(tert-butoxycarbonylamino)-3-(1H-indol-3-yl)propanoate
  • (S)-2-tert-Butoxycarbonylamino-3-(-1H-indol-3-yl)propionic acid benzyl ester
  • Boc-L-Trp-OBzl
CAS:
57229-67-1
MF:
C23H26N2O4
MW:
394.46
Mol File:
57229-67-1.mol
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BOC-TRP-OBZL Chemical Properties

Melting point:
140-146℃
Boiling point:
591.0±50.0 °C(Predicted)
Density 
1.205±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
form 
Powder
pka
11.14±0.46(Predicted)
color 
Off-white to white
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BOC-TRP-OBZL Usage And Synthesis

Chemical Properties

White to off-white powder

Synthesis

100-39-0

13139-14-5

57229-67-1

General procedure for the synthesis of N-tert-butoxycarbonyl-O-benzyl-L-tryptophan from benzyl bromide and (S)-2-((tert-butoxycarbonyl)amino)-3-(1H-indol-3-yl)propanoic acid: to a solution of methyl (S)-2-((tert-butoxycarbonyl)amino)-3-(1H-indol-3-yl)propanoate (2 g, 6.57 mmol) in DMF (27 mL) K2CO3 (2.27 g, 16.5 mmol) and benzyl bromide (811 μL, 6.83 mmol) were added to it. The reaction mixture was stirred at room temperature for 12 hours. After completion of the reaction, the reaction was quenched with saturated aqueous NaHCO3 solution. The reaction mixture was diluted with EtOAc (10 mL) and washed with aqueous NH4Cl to separate the organic and aqueous layers. The aqueous layer was extracted with EtOAc (3 x 10 mL), the organic layers were combined, washed with brine (3 x 15 mL), dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. A white powdery product (2.1 g, 81% yield) was obtained by recrystallization from cyclohexane with a melting point of 140 °C. The spectral data of the product were in agreement with those reported in the literature.1H NMR (250 MHz, CDCl3): δ=8.00 (br s, 1H), 7.56 (d, J=8.3 Hz, 1H), 7.38-7.30 (m, 4H), 7.29-7.17 (m, 3H), 7.16-7.07 (m, 1H), 6.81 (s, 1H), and 5.09 (d, J=3.7Hz, 2H), 4.79-4.61 (m, 1H), 3.29 (d, J=5.3Hz, 2H), 1.43 (s, 9H).

References

[1] Organic and Biomolecular Chemistry, 2013, vol. 11, # 10, p. 1594 - 1597
[2] Journal of Organic Chemistry, 2014, vol. 79, # 23, p. 11549 - 11557
[3] Tetrahedron Letters, 2009, vol. 50, # 26, p. 3645 - 3647
[4] Synthesis (Germany), 2017, vol. 49, # 2, p. 391 - 396
[5] Carbohydrate Research, 1981, vol. 89, p. 229 - 236

BOC-TRP-OBZLSupplier

Shanghai Hanhong Scientific Co.,Ltd.
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