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HRID 343273作成日:2026年10月26日

Sodium Carbonate → 1-(Tetrahydro-2-furoyl)piperazine

https://huagongshe.com/reaction/343273

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物Sodium HydroxideHCID 14798—
反応物1-(2-Furoyl)piperazineHCID 550206—
反応物1-(2-Tetrahydrofuroyl)piperazine hydrobromideHCID 16217252—
触媒NickelHCID 935—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物1-(Tetrahydro-2-furoyl)piperazineHCID 2734641—

反応手順

The furoylpiperazine of Example 1 was converted to the hydrobromide salt (m.p. 173°-175° C.). This salt (39.0 g) in 250 ml methyl alcohol and 9.0 g Raney nickel was hydrogenated at 3 atm. After uptake of H2 ceased, the catalyst was filtered, the solvent concentrated, and the residue crystallized from isopropyl alcohol to give 35.2 g. tetrahydrofuroylpiperazine HBr, m.p. 152°-156° C. This was suspended in 20 ml H2O. Then 10.5 g 50%, NaOH solution was added slowly followed by 2.0 g solid Na2CO3. This was extracted with 4×100 ml portions of warm CHCl3. The CHCl3 extractions were distilled to give 22.5 g tetrahydrofurolylpiperazine, b.p. 120°-125° C./0.2 mm Hg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05861309
出典データセットuspto-grants-1999_01
ORD IDord-0ce1210b61264f4391e1f370710c5052
出典メモuspto-grants-1999_01