|
|
| | (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 | | EINECS: | | | Product Categories: | | | Mol File: | 77119-85-8.mol |  |
| | (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 Rotation | [α]20/D +45°, c = 0.5 in methanol | | Major Application | peptide synthesis | | InChI | 1S/C14H19NO3/c1-14(2,3)18-13(17)15-12(10-16)9-11-7-5-4-6-8-11/h4-8,10,12H,9H2,1-3H3,(H,15,17)/t12-/m1/s1 | | InChIKey | ZJTYRNPLVNMVPQ-GFCCVEGCSA-N | | SMILES | [H]C(=O)[C@@H](Cc1ccccc1)NC(=O)OC(C)(C)C |
| WGK Germany | 3 | | HS Code | 29223900 | | Storage Class | 13 - Non Combustible Solids |
| | (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 | 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-PHENYLPROPANAL Preparation Products And Raw materials |
|