HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131649Generated: October 29, 2026
Dimethylformamide → HCID 23117348, compound
https://huagongshe.com/reaction/131649
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 23117349 | HCID 23117349 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 23117348 | HCID 23117348 | — |
Reaction Steps
0.46 mL of butyl iodide and 0.83 g of potassium carbonate were added to a 10 mL dimethylformamide solution of 0.5 g of the compound obtained in Example 39, and the system was stirred for 2 hours at 80° C. After the reaction, water was added and extraction was performed with ethyl acetate. The extracted organic layer was washed with saturated brine, dried with magnesium sulfate, and then subjected to reduced-pressure solvent distillation. The residue thus obtained was refined by silica gel column chromatography (10% ethyl acetate/hexane) and then recrystallized with ethanol to obtain 0.48 g of 2-acetyl-4,5-dihydro-7-(n-butyloxy)naphtho[1,2-b]thiophene (Table 7-1) in the form of yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07384974B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-965826e33f8d4e918402e21fc4f430c3 |
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| Source note | uspto-grants-2008_06 |
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