Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Organic Chemistry >  Carboxylic acids and derivatives >  (R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL

(R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL

Basic information Safety Supplier Related

(R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL Basic information

Product Name:
(R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL
Synonyms:
  • BOC-D-PHENYLALANINAL
  • N-T-BOC-D-PHENYLALANINAL
  • N-BOC-D-PHENYLALANINAL
  • (R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL
  • (R)-(+)-2-(tert-butoxycarbonylamino)-3-phenylprop
  • N-BOC-D-Phenylalaninal,97%
  • N-Boc-D-phenylalaninal 97%
  • tert-butyl(R)-(1-oxo-3-phenylpropan-2-yl)carbamate
CAS:
77119-85-8
MF:
C14H19NO3
MW:
249.31
Mol File:
77119-85-8.mol
More
Less

(R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL Chemical Properties

Melting point:
86-89 °C (lit.)
storage temp. 
-20°C
form 
Crystalline Powder
color 
White or tan
optical activity
[α]20/D +45°, c = 0.5 in methanol
More
Less

Safety Information

WGK Germany 
3
HS Code 
29223900

MSDS

More
Less

(R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANAL Usage And Synthesis

Chemical Properties

White or tan crystalline powder

Uses

Boc-D-phenylalaninal is a useful research chemical compound used as a reactant in the copper(I)-catalyzed synthesis of 1,2,3-triazoles as inhibitors of human immunodeficiency virus type 1 protease.

reaction suitability

reaction type: Boc solid-phase peptide synthesis

Synthesis

19901-50-9

77119-85-8

A toluene solution of DIBAL-H (1.0 M, 179 mL, 179 mmol) was added slowly and dropwise to a toluene-DCM (4:1, 1000 mL) solution of Compound 31c (25.0 g, 90 mmol) under stirring at -78 °C. The reaction was carried out under argon protection, followed by slow warming to room temperature and continuous stirring at this temperature for 1 hour. Immediately after completion of the reaction, methanol (200 mL) was added to quench the reaction. The reaction mixture was poured into 200 mL of 20% aqueous sodium potassium tartrate (Rochelle salt) and stirred at room temperature until the two phases were clearly separated. The organic layer was separated, concentrated under vacuum and the residue was purified by column chromatography (eluent: hexane/ethyl acetate = 2:1) to afford the target product compound 31d as a white solid (19.9 g, 89% yield).

References

[1] Patent: WO2011/107248, 2011, A1. Location in patent: Page/Page column 68; 69
[2] Journal of Medicinal Chemistry, 1993, vol. 36, # 2, p. 211 - 220
[3] Heterocycles, 1998, vol. 48, # 7, p. 1331 - 1335
[4] The Journal of organic chemistry, 2002, vol. 67, # 17, p. 6162 - 6173
[5] Journal of the Chemical Society - Perkin Transactions 1, 1999, # 20, p. 2983 - 2996

(R)-(+)-2-(TERT-BUTOXYCARBONYLAMINO)-3-PHENYLPROPANALSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Email
market03@meryer.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Capot Chemical Co., Ltd
Tel
+86 (0) 571 85 58 67 18
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com