HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840873Generated: October 31, 2026
1-Iodohexane → 2(1H)-Quinolinone, 6-acetyl-1-hexyl-3,4-dihydro-4,4-dimethyl-
https://huagongshe.com/reaction/1840873
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Iodohexane | HCID 12527 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Acetyl-4,4-dimethyl-3,4-dihydroquinolin-2(1H)-one | HCID 23444702 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2(1H)-Quinolinone, 6-acetyl-1-hexyl-3,4-dihydro-4,4-dimethyl- | HCID 12135416 | 31% |
Reaction Steps
Sodium hydride (21 mg, 90 mmol) was slowly added into a solution of 6-acetyl-4,4-dimethyl-3,4-dihydro-1H-quinolin-2-one (Intermediate 5, 98 mg, 45 mmol) in 3 mL of DMF at 0° C. After stirring at 0° C. for 10 min, 1-iodo-n-hexane (29 mg, 135 mmol) was added to the reaction mixture and the ice-bath was removed. The reaction was allowed to stir for 2 h before quenching 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 as a colorless oil (41.8 mg, 31% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06683092B1 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-618af945b3e5410287c4ed2e02da2b5d |
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| Source note | uspto-grants-2004_01 |
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