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HRID 327585作成日:2026年10月27日

Phenoxyacetic Acid → 2-[N-n-propyl,N-2-(phenyloxy)ethylamino]-5-methoxytetralin

https://huagongshe.com/reaction/327585

反応式

関与物質

役割名称HCID仕込み量
反応物Phenoxyacetic AcidHCID 19188—
反応物Borane,N-dimethylmethanamine (1:1)HCID 6327651—
反応物2-Propylamino-5-methoxytetralinHCID 10242548—
溶媒Diethyl EtherHCID 3283—
生成物2-[N-n-propyl,N-2-(phenyloxy)ethylamino]-5-methoxytetralinHCID 15228850—

反応手順

A mixture of 2-(N-n-propylamino)-5-methoxytetralin (7.0 g, 0 0319 mol; prepared according to J. Chem. Soc., 1965, pp. 26-36), phenoxyacetic acid (4.86 g, 0.0319 mol), and borane trimethylamine complex (2.33 g, 0.0319 mol) was refluxed in xylenes overnight. The cooled reaction mixture was extracted with NaHCO3 and the organic layer was dried over MgSO4, filtered and concentrated under reduced pressure. The resulting oil was subjected to flash chromatography (silica; 9:1 pet ether/EtOAc) and product was isolated: NMR of the free base (300 MHz, CDCl3): δ 7.3-6.6(m, 8H), 4.0(t, 2H), 3.7(s, 3H), 3.1-2.5(m, 9H), 2.1(m, 1H), 1.7-1.4(m, 3H), 0.9(t, 3H). The free base thus isolated was converted to hydrochloride salt by the addition of dry ether-HCL.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05274003
出典データセットuspto-grants-1993_12
ORD IDord-adb00b0532464acfa885f84695ff13dc
出典メモuspto-grants-1993_12