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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250231Generated: October 31, 2026

4-Chlorobenzaldehyde → HCID 70164883, compound

https://huagongshe.com/reaction/1250231

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantHCID 18327332HCID 18327332—
SolventAcetic AcidHCID 176—
ProductHCID 70164883HCID 70164883—

Reaction Steps

A solution of the product from Step C (144 mg, 0.33 mmol) and 4-chlorobenzaldehyde (46 mg, 0.33 mmol) in acetic acid (15 mL) was heated at 120° C. for 17 h. The reaction mixture was concentrated under vacuum and the residue was diluted with CHCl3. The organic solution was washed with sat'd aq NaHCO3, sat'd aq NaCl, dried and concentrated. Purification via SiO2-gel chromatography using EtOAc/NEt3 (10:1) yielded the desired product. API-MS: 563 (M+1). 1H NMR (300 MHz, CDCl3): d 8.0 (d, 2 H), 7.8 (d, 1 H), 7.5 (d, 2 H), 7.38 (m, 3 H), 7.15 (d, 1 H), 7.0 (d, 2 H), 4.1 (t, 2 H), 4.0 (s, 3 H), 2.85 (m), 2.3 (m), 1.9-1.2 (m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06337332B1
Source datasetuspto-grants-2002_01
ORD IDord-05c58666ceb24052a08b17ddcf78dd7f
Source noteuspto-grants-2002_01