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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 327585생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/327585

반응식

참여 물질

역할이름HCID투입량
반응물Phenoxyacetic AcidHCID 19188—
반응물Borane,N-dimethylmethanamine (1:1)HCID 6327651—
반응물2-Propylamino-5-methoxytetralinHCID 10242548—
용매Diethyl EtherHCID 3283—
생성물2-[N-n-propyl,N-2-(phenyloxy)ethylamino]-5-methoxytetralinHCID 15228850—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05274003
출처 데이터셋uspto-grants-1993_12
ORD IDord-adb00b0532464acfa885f84695ff13dc
출처 메모uspto-grants-1993_12