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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217065Generated: October 30, 2026

Sodium Hydroxide → HCID 10132918, compound

https://huagongshe.com/reaction/2217065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1-(3,5-Dimethoxyphenyl)ethan-1-oneHCID 95997—
ReactantHCID 21946174HCID 21946174—
SolventMethanolHCID 887—
ProductHCID 10132918HCID 1013291850%

Reaction Steps

A mixture of 3-hydroxy-4-butoxybenzaldehyde (0.4 g, 2.1 mmol), 3,5-dimethoxyacetophenone (0.371.9, 2.1 mmol) and 50% w/v of aqueous sodium hydroxide (3.3 ml, 0.206 mol) in methanol (10 ml) at room temperature for 18 h. The yellow solid that precipitated was filtered and sequentially washed with cold methanol and ether and finally dried in a vacuum dessicator. Purification was achieved using column chromatography (SiO2, petroleum:ether (40:60 v/v) with an increasing gradient of ethyl acetate) which gave 0.36 g (50%) of a yellow solid: 1H-NMR (CDCl3) δ 7.7 (d, 1H), 7.3 (m, 2H), 7.1 (d, 3H), 6.8 (d, 1H), 6.7 (t, 1H), 5.7 (s, 1H), 4.1 (t, 2H), 3.9 (s, 6H), 1.8 (m, 2H), 1.5 (m, 2H), 1.0 (t, 3H). 13C-NMR (CDCl3) δ 190.0, 160.9, 148.3, 146.0, 144.9, 140.5, 128.4, 122.6, 120.2, 112.9, 111.4, 106.2, 104.9, 68.8, 55.6, 31.1, 19.1. 13.7. Mass Spectrum m/e (M+1) 357. Anal. Calcd. for C21H24O5: C, 70.77, H, 6.79. Found C, 70.84; H, 6.81.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112698B2
Source datasetuspto-grants-2006_09
ORD IDord-4e517f95742e4ecba09c70d2ffc46d59
Source noteuspto-grants-2006_09