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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 395678Generated: November 2, 2026

3-Chloro-4-hydroxybenzaldehyde → HCID 21352697, compound

https://huagongshe.com/reaction/395678

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-4-hydroxybenzaldehydeHCID 17022—
ReactantHCID 53635745HCID 53635745—
ProductHCID 21352697HCID 21352697—

Reaction Steps

Using the general procedure described in Example 3, N1-(4-methoxybenzoyl)-N2-(piperidin-4-ylcarbonyl)-1,2-benzenediamine (0.045 mmol) was reacted with 3-chloro-4-hydroxybenzaldehyde to provide 22 mg of the title product as the free base. Treatment with hydrochloric acid and concentration in vacuo yielded the salt of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06605626B2
Source datasetuspto-grants-2003_08
ORD IDord-03b99ad3f0fd4412b15786cce05bebde
Source noteuspto-grants-2003_08