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| | Cbz-alpha-allyl-L-Gly Basic information |
| Product Name: | Cbz-alpha-allyl-L-Gly | | Synonyms: | N-ALPHA-CARBOBENZOXY-L-ALPHA-ALLYL-GLYCINE;RARECHEM AL CF 0941;Z-ALGLY-OH;A-(ALLYL)GLY-OH;CBZ-(S)-2-AMINO-4-PENTENOIC ACID;(S)-2-CBZ-AMINO-4-PENTENOIC ACID;L-CBZ-ALLYLGLYCINE;Z-(ALLYL)GLY-OH | | CAS: | 78553-51-2 | | MF: | C13H15NO4 | | MW: | 249.26 | | EINECS: | | | Product Categories: | | | Mol File: | 78553-51-2.mol |  |
| | Cbz-alpha-allyl-L-Gly Chemical Properties |
| Melting point | 240-245 °C (decomp) | | Boiling point | 444.967±45.00 °C(Press: 760.00 Torr)(predicted) | | density | 1.203±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted) | | storage temp. | 2-8°C | | form | Solid | | pka | 3.816±0.10(predicted) | | color | White to off-white | | Optical Rotation | Consistent with structure |
| | Cbz-alpha-allyl-L-Gly Usage And Synthesis |
| Uses | (2S)-2-[[(phenylmethoxy)carbonyl]amino]-4-Pentenoic acid is a useful building block, and has been used in the regioselective preparation of nonracemic silylated amino acids. | | Synthesis | (S)-(-)-2-Amino-4-pentenoic acid (2.0 g) was suspended in dioxane (80 mL) at room temperature and triethylamine (4.3 g), water (2.0 mL) and N-(phenylmethoxycarbonyloxy)succinimide (9.1 g) were added sequentially. The reaction mixture was stirred overnight at room temperature and then concentrated under vacuum. Subsequently, the reaction mixture was diluted with saturated NaHCO3 solution and extracted with ether (3 x 80 mL). The basic aqueous layer was acidified to pH 2 with 2N HCl and extracted with EtOAc (3 x 80 mL). The EtOAc layers were combined, washed with brine, dried over anhydrous Na2SO4, filtered and the solvent evaporated. Finally, a viscous oily product (4.41 g, quantitative yield) was obtained by concentration from toluene (2 × 20 mL). The product was confirmed by 1H NMR (300 MHz, DMSO-d6): δ 2.31-2.50 (m, 2H), 4.00-4.06 (m, 1H), 5.03 (s, 2H), 5.05-5.12 (m, 2H), 5.71-5.84 (m, 1H), 7.35 (m, 5H), 7.53 (d, 1H), 12.57 (bs, 1H). Mass spectrometry analysis (APCI) showed m/z = 250 ([M+H]+).LC/MS analysis (Method A) showed a retention time of 2.30 min. | | References | [1] Patent: WO2004/80983, 2004, A1. Location in patent: Page 47
[2] Tetrahedron, 2013, vol. 69, # 30, p. 6275 - 6284
[3] Organic Letters, 2006, vol. 8, # 2, p. 239 - 242
[4] Patent: WO2011/15241, 2011, A1. Location in patent: Page/Page column 187; 398
[5] Patent: US2012/270881, 2012, A1. Location in patent: Page/Page column 116 |
| | Cbz-alpha-allyl-L-Gly Preparation Products And Raw materials |
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