Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179513Generated: October 27, 2026

Hydrochloric Acid → 1-(3,4-Dimethoxy-1-naphthyl)-8-(4-aminophenyl)-octane

https://huagongshe.com/reaction/1179513

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-(3,4-Dimethoxy-1-naphthyl)-8-(4-acetamidophenyl)-octaneHCID 22647802—
SolventMethanolHCID 887—
Product1-(3,4-Dimethoxy-1-naphthyl)-8-(4-aminophenyl)-octaneHCID 2264779575%

Reaction Steps

A solution of 554.6 mg (1.28 mmol) of 1-(3,4-dimethoxy-1-naphthyl)-8-(4-acetamidophenyl)-octane in 20 mL of MeOH was mixed with 21 mL of 2N HCl. The reaction mixture was refluxed for 23 hr. Then the reaction mixture was partitioned between 75 mL of CH2Cl2 and 21 mL of 2N NaOH. The aqueous phase was extracted with CH2Cl2 (5×40 mL). The CH2Cl2 extracts were combined, dried with MgSO4, and evaporated to dryness. Column chromatography on silica gel with 1% MeOH in CH2Cl2 gave 374.6 mg (75%) of aniline 537: 1H NMR (250 MHz, CDCl3, TMS) δ 8.14 (d, J=8 Hz, 1H), 7.94 (d, J=8 Hz, 1H), 7.47 (t, J=8 Hz, 1H), 7.37 (t, J=8 Hz, 1H), 7.12 (s, 1H), 6.96 (d, J=8 Hz, 2H), 6.62 (d, J=8 Hz, 2H), 3.99 (s, 3H), 3.97 (s, 3H), 3.1-3.0 (m, 2H), 2.5-2.4 (m, 2H), 1.8-1.3 (m 12H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279502B2
Source datasetuspto-grants-2007_10
ORD IDord-7bf5d72e763446ea95c6298a55959758
Source noteuspto-grants-2007_10