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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327587Generated: October 24, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenoxyacetic AcidHCID 19188—
ReactantBorane,N-dimethylmethanamine (1:1)HCID 6327651—
Reactant2-Propylamino-5-methoxytetralinHCID 10242548—
Product2-[N-n-propyl,N-2-(phenyloxy)ethylamino]-5-methoxytetralinHCID 15228850—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05274003
Source datasetuspto-grants-1993_12
ORD IDord-d00fd4a5353845a58ddd8c8f0af6d863
Source noteuspto-grants-1993_12