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HRID 1600525作成日:2026年10月24日

Hydrochloric Acid → Boc-homophenylalaninal

https://huagongshe.com/ja/reaction/1600525

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物4-MethylmorpholineHCID 7972—
反応物Isobutyl chloroformateHCID 62365—
反応物CP 84364HCID 664657—
反応物ethyl (S)-4-amino-6-phenyl-2-hexenoate hydrochlorideHCID 86754733—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物Boc-homophenylalaninalHCID 1026474080%

反応手順

Morpholinecarbonylphenylalanine (2.74 g, 9.82 mmol, prepared according to the method described in Esser, R. et.al., Arthritis & Rheumatism (1994), 0000) was dissolved in THF (50 mL) at -10° C. 4-methylmorpholine (1.08 mL, 9.82 mmol) was added, followed by isobutyl chloroformate (1.27 mL, 9.82 mmol). The mixed anhydride was stirred for 10 minutes, whereupon a solution of ethyl (S)-4-amino-6-phenyl-2-hexenoate hydrochloride from the previous step in DMF (10 mL) was added, followed by 4-methylmorpholine (1.08 mL, 9.82 mmol). The mixture was stirred for 1 hour. 1M HCl (50 mL) was added. The product was extracted with ethyl acetate (100 mL), washed with saturated aqueous NaHCO3 (50 mL), dried over MgSO4 and decolorizing charcoal (DARCO), filtered, and evaporated to dryness, giving 3.80 g (80% yield from Boc-homophenylalaninal).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05976858
出典データセットuspto-grants-1999_11
ORD IDord-acf3b734ba6c4d49893738d6d94827e3
出典メモuspto-grants-1999_11