4-Chloro-3,5-dinitrobenzotrifluoride → HCID 59293622, compound

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Reaction Steps

(R)-3-hydroxypyrrolidine-1-carboxylic acid tert-butyl ester is de-protonated with potassium tert-butoxide (KOtBu) in tetrahydrofuran (THF). The resulting anion is reacted with 2-chloro-1,3-dinitro-5-trifluoromethylbenzene in tert-butyl methyl ether (MTBE)/THF. When the reaction is complete, the reaction mixture is quenched with water and partitioned with more MTBE. The organic layer is washed with brine and water and concentrated on a rotary evaporator. The solid concentrate is re-dissolved in methanol and re-precipitated with water. The resulting precipitate is filtered and dried to afford (R)-3-(2,6-dinitro-4-trifluoromethylphenoxy)pyrrolidine-1-carboxylic acid tert-butyl ester which can be used in the next step without further purification.

Provenance & Evidence