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HRID 37039作成日:2026年10月23日

Trityl chloride → N-triphenylmethyl-alpha-aminobutyrolactone

https://huagongshe.com/ja/reaction/37039

反応式

関与物質

役割名称HCID仕込み量
反応物Trityl chlorideHCID 6456—
反応物4-MethylmorpholineHCID 7972—
反応物Homoserine lactone hydrobromideHCID 73508—
溶媒DimethylformamideHCID 6228—
生成物N-triphenylmethyl-alpha-aminobutyrolactoneHCID 13856082—

反応手順

α-Aminobutyrolactone hydrobromide (10.0 g, 54.9 mmol), N-methylmorpholine (11.2 g, 110.0 mmol) and triphenylmethyl chloride (15.4 g, 55.2 mmol) were dissolved in N,N-dimethylformamide (DMF) (200 ml) (distilled from calcium hydride) and stirred at ambient temperature for 16 hours. The mixture was filtered, and water (200 ml) was added to the DMF-solution. The resulting slurry was stirred for 2 hours, the precipitate was filtered off and washed with a mixutre of DMF and water (1:1, 50 ml). The solid was resuspended in water (100 ml), filtered and dried at 50° C. in vacuo. N-triphenylmethyl-α-amino-butyrolactone was isolated as a white solid. Yield 17.55 g (93.2%), mp 164.5°-165.5° C. (uncorrected).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05419893
出典データセットuspto-grants-1995_05
ORD IDord-53b464ac8a92404eaf0cf1fbc086b494
出典メモuspto-grants-1995_05