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| | N-(Trifluoroacetyl)glycine Basic information |
| | N-(Trifluoroacetyl)glycine Chemical Properties |
| Melting point | 120-121 °C | | Boiling point | 291.6°C | | density | 1.534 | | Fp | 130°C | | storage temp. | Sealed in dry,Room Temperature | | solubility | Chloroform, DMSO | | form | Solid | | pka | 2.99±0.10(Predicted) | | color | White | | InChI | InChI=1S/C4H4F3NO3/c5-4(6,7)3(11)8-1-2(9)10/h1H2,(H,8,11)(H,9,10) | | InChIKey | IFAXXCBMQJNCCF-UHFFFAOYSA-N | | SMILES | C(O)(=O)CNC(C(F)(F)F)=O | | CAS DataBase Reference | 383-70-0 | | NIST Chemistry Reference | N-(Trifluoroacetyl)aminoacetic acid(383-70-0) |
| | N-(Trifluoroacetyl)glycine Usage And Synthesis |
| Chemical Properties | White Solid | | Uses | N-Trifluoroacetylglycine (cas# 383-70-0) is a compound useful in organic synthesis. | | Definition | ChEBI: N-(trifluoroacetyl)glycine is an N-acylglycine resulting from the formal condensation of the amino group of glycine with the carboxy group of trifluoroacetic acid. It is a N-acylglycine, a secondary carboxamide and a trifluoroacetamide. | | Synthesis | The general procedure for the synthesis of 2-(2,2,2-trifluoroacetamido)acetic acid from ethyl trifluoroacetate and glycine was carried out as follows: the TFA-α-amino acid was prepared by the method reported in references [1,2] with slight modifications. First, triethylamine (33 mmol, 1.5 eq.) was added to a methanolic solution (22 mL) of glycine (22 mmol). after 5 min, ethyl trifluoroacetate (29 mmol, 1.3 eq.) was added and the reaction mixture was stirred for 24 h. The reaction was carried out by rotary evaporation. Upon completion of the reaction, the solvent was removed by rotary evaporation. The remaining residue was dissolved in water (35 mL) and acidified with concentrated hydrochloric acid (4 mL). After acidification, the mixture was stirred for 15 minutes and then extracted with ethyl acetate. The organic layers were combined, washed sequentially with water and brine, and dried with anhydrous magnesium sulfate. After drying, filter and concentrate by rotary evaporation. If cured products (e.g., L-1a, D-1a, L-2a, D-2a, 3a, L-4a, D-4a to D-8a) are desired, they can be further dried overnight under high vacuum. | | References | [1] Organic and Biomolecular Chemistry, 2015, vol. 13, # 30, p. 8298 - 8309
[2] Organic Letters, 2018, vol. 20, # 18, p. 5877 - 5880
[3] Molecules, 2017, vol. 22, # 10,
[4] European Journal of Organic Chemistry, 2012, # 29, p. 5774 - 5788,15
[5] European Journal of Organic Chemistry, 2012, # 29, p. 5774 - 5788 |
| | N-(Trifluoroacetyl)glycine Preparation Products And Raw materials |
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