HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324891Generated: October 30, 2026
3,5-Heptanedione → HCID 22005256, compound
https://huagongshe.com/reaction/324891
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3,5-Heptanedione | HCID 81923 | — |
| Reactant | Bis(1,1-dimethylethyl) 3-oxoglutarate | HCID 119788 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22005256 | HCID 22005256 | 97.5% |
Reaction Steps
A mixture of di-tert-butyl 1,3-acetonedicarboxylate (10 g, 38.7 mmol), 3,5-heptanedione (6.5 g, 50.3 mmol) and sodium methoxide (2.7 g, 50.3 mmol) in methanol (100 mL) was stirred at room temperature overnight. Methanol was removed via rotary evaporation and the resulting orange sludge was partitioned between diethyl ether (100 mL) and 10% aqueous hydrochloric acid (100 mL). The separated aqueous layer was extracted with diethyl ether (50 mL×2). The combined organic portions were washed with saturated aqueous sodium chloride (20 mL), dried over sodium sulfate, filtered through a pad of silica (20 mm×40 mm) and concentrated in vacuo to yield a yellow oil (13.23 g, 97%): 1H NMR (300 MHz, CDCl3): δ 1.20 (t, 6H), 1.60 (s, 18H) 2.74 (q, 4H), 6.55 (s, 1H), 11.73 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06218431B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-ae61b28b19e14a8ba073f2fd1cddf87a |
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| Source note | uspto-grants-2001_04 |
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