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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032892Generated: November 1, 2026

Hexane → HCID 136156243, compound

https://huagongshe.com/reaction/1032892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantEthyl AcetateHCID 8857—
Reactant(S)-Benzyl (1-(cyclohexylamino)-3-methyl-1-oxobutan-2-yl)carbamateHCID 826228—
Reactant2-Formyl-6-phenylphenolHCID 10703100—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 136156243HCID 13615624376.6%

Reaction Steps

The carbobenzoxy-(S)-valine cyclohexylamide (0.33 g, 1 mmol) was dissolved in methanol (30 ml) and the solution was stirred at room temperature for 3 hours in the presence of 5% palladium-carbon (30 mg) under a hydrogen gas atmosphere. After the reaction was over, the palladium-carbon catalyst was filtered off to obtain a colorless solution. To this solution was added 3-phenylsalicylaldehyde (0.22 g, 1.1 mmol). This solution was stirred at room temperature for 24 hours and concentrated under reduced pressure to obtain yellow solids. These solids were subjected to silica gel column chromatography (eluent; hexane:ethyl acetate=5:1) to obtain 0.29 g (76%) of the desired N-(3-phenylsalicylidene)-(S)-valine cyclohexylamide which was further recrystallized from ether. m.p. 87.0°-89.5° C. [α]26D +158.3° (c 1.02, CHCl3)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05308820
Source datasetuspto-grants-1994_05
ORD IDord-1d490d2fca0d4039ad4851e2102700db
Source noteuspto-grants-1994_05