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HRID 1659645作成日:2026年10月25日

1-Phenethylamine → Flurbiprofen

https://huagongshe.com/reaction/1659645

反応式

関与物質

役割名称HCID仕込み量
反応物1-PhenethylamineHCID 7408—
反応物Diisooctyl phthalateHCID 33934—
反応物2-(2-Fluoro-4-biphenylyl)acrylic acidHCID 20559788—
溶媒BenzeneHCID 241—
溶媒EthanolHCID 702—
生成物FlurbiprofenHCID 3394—

反応手順

DIOP (64.8 mg.) was added to a solution of DTDR (46 mg.) in benzene (9 ml.) under nitrogen and the mixture allowed to stand for 15 minutes. This complex was then added to a mixture, prepared by adding ethanol (16 ml.) followed by (-)-α-methylbenzylamine (24 mg.) in ethanol (2 ml.) to the product of Example 2 (0.5 g.), under hydrogen. The reaction mixture was stirred under hydrogen for 51/2 hours at room temperature and then kept under hydrogen overnight. The solution was concentrated under reduced pressure and the residue treated with ether and aqueous 10% potassium carbonate. The ether extract was treated with the potassium carbonate extract, which was then acidified. The oil which separated, solidified and was extracted with ether and the extract dried, filtered, evaporated and the product recrystallised from light petroleum (b.p. 60°-80° C.) to give 2-(2-fluoro-4-biphenylyl)propionic acid, m.p. 101°-103° C., having an optical rotation [α]D20 +35.5° C. representing 89% of the (+) isomer in the product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04304931
出典データセットuspto-grants-1981_12
ORD IDord-51c4fbec21c346febe5d604e9f49c908
出典メモuspto-grants-1981_12