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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1682249Generated: October 29, 2026

Toluene → HCID 19937045, compound

https://huagongshe.com/reaction/1682249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPiperidineHCID 8082—
Reactantdi-(2-ethylhexyl) malonateHCID 9923500—
ReactantHCID 11217997HCID 11217997—
SolventAcetic AcidHCID 176—
ProductHCID 19937045HCID 1993704564%

Reaction Steps

A mixture of 3™allyl-4,5-dimethoxybenzaldehyde (10.3 g, 0.05 moles), di-(2-ethylhexyl) malonate (16.4 g, 0.05 moles), toluene (20 ml), acetic acid (0.41 ml) and piperidine (0.77 ml) is heated to reflux using a Dean Stark. After cooling, washing the toluene phase with water, drying and evaporation of the solvent, an orange-coloured oil is obtained, which is purified by chromatography on a column of silica 60 (eluent: 90:10 heptane/ethyl acetate) to give di-(2-ethylhexyl) 3-allyl-4,5-dimethoxybenzalmalonate (colourless oil, 15 g, yield=64%), which has the following characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05175340
Source datasetuspto-grants-1992_12
ORD IDord-d725a560384140638fb515d85c326714
Source noteuspto-grants-1992_12