HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352621Generated: October 28, 2026
1,2-Cyclohexanedione → HCID 178439981, compound
https://huagongshe.com/reaction/2352621
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Cyclohexanedione | HCID 13006 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | L-Norvalinamide--hydrogen chloride (1/1) | HCID 56777018 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178439981 | HCID 178439981 | 50% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04877877 |
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| Source dataset | uspto-grants-1989_10 |
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| ORD ID | ord-bc94c18fc10549209fcb7718d1720408 |
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| Source note | uspto-grants-1989_10 |
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