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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222332Generated: October 30, 2026

3,4-Dimethoxybenzeneacetonitrile → HCID 10267333, compound

https://huagongshe.com/reaction/2222332

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DimethoxybenzeneacetonitrileHCID 66727—
ReactantHCID 23046188HCID 23046188—
ProductHCID 10267333HCID 1026733357.8%

Reaction Steps

The hydroxyl group of 3,5-dimethyl-4-hydroxybenzaldehyde (2.3 g) was protected by use of 2-methoxyethoxymethyl chloride (3.4 g) in accordance with (production process 1), to thereby produce 3,5-dimethyl-4-methoxyethoxymethoxybenzaldehyde (2.7 g, yield: 62%). The thus-produced 3,5-dimethyl-4-methoxyethoxymethoxybenzaldehyde (2.0 g) and 3,4-dimethoxybenzyl cyanide (1.5 g) were subjected to condensation in accordance with process A of (production process 2), to thereby yield an MEM form of the target product. Subsequently, the protective group was removed from the MEM form in accordance with (production process 3), to thereby produce the target product (1.5 g, yield: 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371773B2
Source datasetuspto-grants-2008_05
ORD IDord-2b571cd0500d4991a4ef6110fc6bc58e
Source noteuspto-grants-2008_05