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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276165Generated: October 25, 2026

Benzaldehyde → Heptanophenone

https://huagongshe.com/reaction/276165

Reaction equation

Participants

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

Reaction Steps

Under the same reaction procedure and conditions as in Example 1 (benzaldehyde 0.5 mmol, 2-amino-3-picoline 0.1mmol, 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 combined with Rh(PPh3)3Cl 1 0.01 mmol. While the reactor was stopped with a stopper, the reactants were stirred at various temperatures (70-130° C.) as shown in the following table 10 for 1 hour. After completion of the reaction, gas chromatography was conducted to determine the yields of heptanophenone, products according to various temperatures and the results are given in Table 10, below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06353139B1
Source datasetuspto-grants-2002_03
ORD IDord-513cbb7ec128432190a40b608fe0b8bb
Source noteuspto-grants-2002_03