HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453631Generated: October 30, 2026
1-Iodoheptane → 6-Acetyl-1-heptyl-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one
https://huagongshe.com/reaction/1453631
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Iodoheptane | HCID 20274 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Acetyl-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one | HCID 23444702 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Acetyl-1-heptyl-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one | HCID 23444699 | 66% |
Reaction Steps
Sodium hydride (21.0 mg, 90.0 mmol) was slowly added into a solution of 6-acetyl-4,4-dimethyl-3,4-dihydro-1H-quinolin-2-one (Compound 28, 98.0 mg, 45.0 mmol) in 3 mL of DMF at 0° C. After stirring at 0° C. for 10 min, 1-iodoheptane (30.5 mg, 135.0 mmol) was added to the reaction mixture and the ice-bath was removed. The reaction mixture was allowed to stir for 2 h and then quenched with ice water. The resulting solution was then extracted with ether (3×10 mL), washed with brine (1×10 mL), dried (MgSO4) and concentrated at reduced pressure. Purification by flash chromatography (75:25 hexane/ethyl acetate) yielded the title compound (93.6 mg, 66% yield) as a colorless oil:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07476673B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-78c5cc729a4149928f1ee9ad359bca33 |
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| Source note | uspto-grants-2009_01 |
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