Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352606Generated: November 1, 2026

1,2-Cyclohexanedione → HCID 178439981, compound

https://huagongshe.com/reaction/2352606

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-CyclohexanedioneHCID 13006—
ReactantSodium HydroxideHCID 14798—
Reactant(2S)-2-aminopentanamide hydrochlorideHCID 56777018—
SolventMethanolHCID 887—
ProductHCID 178439981HCID 17843998150%

Reaction Conditions

Temperature-30 °C

Reaction Steps

1,2-cyclohexanedione (5.4 g, 48 mM) was added all at once to a methanol solution (80 ml) of norvalineamide hydrochloride (6.1 g, 40 mM) at -30° C., and aqueous 12.5N NaOH (8 ml) was added dropwise thereto. The reaction mixture was stirred at -30° C. for 30 mins., cooling was removed, and the mixture stirred at room temperature for 3 hours. Conc. hydrochloric acid (10 ml) was added to the reaction mixture under ice-cooling, sodium bicarbonate (8 g) was added after 10 mins., the methanol then being distilled off in vacuo. The residue was extracted with chloroform, and the extract washed with water, dried with anhydrous sodium sulfate and concentrated in vacuo. The residue was washed with acetone and recrystallized from acetone to obtain the product as colorless crystals (3.8 g., yield: 50%, m.p.: 131°-133° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04877875
Source datasetuspto-grants-1989_10
ORD IDord-f3ea383d20074b7dbc226ca3c33a5d13
Source noteuspto-grants-1989_10