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BOC-D-TRYPTOPHANOL

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BOC-D-TRYPTOPHANOL Basic information

Product Name:
BOC-D-TRYPTOPHANOL
Synonyms:
  • BOC-(R)-2-AMINO-3-(3-INDOLYL)-1-PROPANOL
  • BOC-D-TRYPTOPHANOL
  • BOC-D-TRP-OL
  • N-BOC-D-TRYPTOPHANOL
  • N-ALPHA-T-BOC-D-TRYPTOPHANOL
  • N-T-BOC-D-TRYPTOPHANOL
  • N-alpha-t-Butyloxycarbonyl-D-tryptophanol
  • (R)-tert-Butyl (1-hydroxy-3-(1H-indol-3-yl)propan-2-yl)carbaMate
CAS:
158932-00-4
MF:
C16H22N2O3
MW:
290.36
Mol File:
158932-00-4.mol
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BOC-D-TRYPTOPHANOL Chemical Properties

Melting point:
119-121℃
Boiling point:
518.1±45.0 °C(Predicted)
Density 
1.190
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
solubility 
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form 
Powder
pka
12.06±0.46(Predicted)
Appearance
White to off-white Solid
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Safety Information

HS Code 
2933499090
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BOC-D-TRYPTOPHANOL Usage And Synthesis

Chemical Properties

White solid

Synthesis

5241-64-5

158932-00-4

General procedure for the synthesis of N-Boc-D-tryptophan from Boc-D-tryptophan: a) Synthesis of compound 22; Compound 1 (Boc-D-tryptophan, 10.0 g, 33 mmol) was dissolved in THF (50 mL), cooled to 0 °C under nitrogen atmosphere, and then BH3/THF solution was slowly added dropwise. The reaction mixture was gradually warmed to room temperature and stirred continuously for 16 hours. Upon completion of the reaction, the reaction was quenched with aqueous potassium carbonate and subsequently extracted with ethyl acetate (100 mL x 3). The organic phases were combined, washed with brine (50 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure. Purification by column chromatography (petroleum ether/ethyl acetate=4:1) afforded the product 22 (N-Boc-D-chromanol) as a white solid (5.72 g, 60% yield).1H NMR (400 MHz, CDCl3): δ1.46 (s, 9H), 3.02 (d, J=6.8 Hz, 2H), 3.80-3.55 (m, 2H). 4.10-3.95 (m, 1H), 4.86 (br s, 1H), 7.07 (s, 1H), 7.16 (t, J=7.2Hz, 1H), 7.23 (t, J=7.2Hz, 1H), 7.39 (d, J=8.4Hz, 1H), 7.68 (d, J=7.6Hz, 1H), 8.20 (s, 1H).

References

[1] ChemMedChem, 2016, p. 1924 - 1935
[2] Patent: WO2012/55945, 2012, A1. Location in patent: Page/Page column 23
[3] Journal of Medicinal Chemistry, 1994, vol. 37, # 13, p. 2011 - 2032

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