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ChemicalBook CAS DataBase List N-TRIFLUOROACETYLGLYCINE, N-SUCCINIMIDYL ESTER
3397-30-6

N-TRIFLUOROACETYLGLYCINE, N-SUCCINIMIDYL ESTER synthesis

2synthesis methods
-

Yield:3397-30-6 100%

Reaction Conditions:

with 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride in dichloromethane at 0;Solvent;

Steps:

3.3. General Procedure for the Preparation of TFA-a-Amino Acid N-Hydroxysuccinimide Ester

General procedure: NHS (N-hydroxysuccinimide, 1.1 equiv.) was added to a solution of TFA--amino acid(L-/D-1a-L-/D-2a, 3a, L-/D-4a-L-/D-8a, 1.0 mmol) in pre-cooled CH2Cl2 (10 mL). The suspensionof WSCD-HCl (water soluble carbodiimide hydrochloride, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide monohydrochloride, 1.0 equiv.) in CH2Cl2 (10 mL) was added drop-wise at 0 Cand the reaction was stirred for 2-4 h. The solvent was removed by rotary evaporation. The residuethat remained was dissolved in ethyl acetate; washed with water, sat. NaHCO3, sat. NaCl, dried overMgSO4, and then evaporated. The product was solidified by washing with hexane to be used for further reaction.

References:

Tachrim, Zetryana Puteri;Oida, Kazuhiro;Ikemoto, Haruka;Ohashi, Fumina;Kurokawa, Natsumi;Hayashi, Kento;Shikanai, Mami;Sakihama, Yasuko;Hashidoko, Yasuyuki;Hashimoto, Makoto [Molecules,2017,vol. 22,# 10,art. no. 1748] Location in patent:supporting information