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HRID 327587作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/327587

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—
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 (80 mg, 31.9 mmol; prepared according to J. Chem. Soc., 1965, pp 26-36), phenoxyacetic acid (166 mg, 109.4 mmol) and borane trimethylamine complex (80 mg, 109.4 mmol) was refluxed in xylenes overnight. The cooled reaction mixture was extracted with NaHCO3 and the organic layer was dried over MgSo4, filtered and concentrated. The resulting oil was subjected to flash chromatography (Silica: 9:1 pet ether/EtOAc) and product was isolated with characteristic peaks at: NMR (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).

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-d00fd4a5353845a58ddd8c8f0af6d863
出典メモuspto-grants-1993_12