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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276161Generated: October 25, 2026

Benzaldehyde → Heptanophenone

https://huagongshe.com/reaction/276161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantBenzoic AcidHCID 243—
ReactantTolueneHCID 1140—
ReactantAnilineHCID 6115—
Reactant1-HexeneHCID 11597—
Reactant2-Amino-3-methylpyridineHCID 15347—
ProductHeptanophenoneHCID 74282—

Reaction Conditions

Temperature130 °C

Reaction Steps

Under the same reaction procedure and conditions as in Example 1 (benzaldehyde 0.5 mmol, 2-amino-3-picoline 0.1 mmol, aniline 0.3 mmol, bezoic acid 0.03 mmol, 1-hexene 2.5 mmol, toluene 0.87 mmol), the mixture in a 500 ml pressure reactor was stirred at normal temperature for 2-3 minutes and then various transition metal catalysts as shown in the following table 6 were added to each reactor. While the reactor was stopped with a stopper, the reactants were heated at 130° C. for 1 hour with stirring. After completion of the reaction, gas chromatography was conducted to determine the yields of heptanophenone, products according to various transition metal catalysts. The results are shown in Table 6, below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06353139B1
Source datasetuspto-grants-2002_03
ORD IDord-0b2b3a60d24044dfbcbd6ee1f35c0342
Source noteuspto-grants-2002_03