HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495004Generated: October 29, 2026
Dimethylformamide → HCID 57682888, compound
https://huagongshe.com/reaction/495004
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Hydroxy-3,4-dihydro-1(2H)-naphthalenone | HCID 4679494 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57682888 | HCID 57682888 | — |
Reaction Steps
830 μl of allyl bromide was added to a mixture consisting of 1.52 g of 6-hydroxy-3,4-dihydronaphthalen-1(2H)-one, 1.22 g of potassium carbonate, and 15 ml of N,N-dimethylformamide. The obtained mixture was stirred at room temperature under nitrogen atmosphere overnight. Water and ethyl acetate were added to the reaction solution, so as to obtain an organic layer. The obtained organic layer was successively washed with water (4 times) and a saturated sodium chloride solution, and then dried over anhydrous sodium sulfate. After removing the drying agent by filtration, the organic layer was concentrated under a reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate), so as to obtain 1.69 g of the subject compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538123B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-6e2a0e0103ad4123838cbe4337287dea |
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| Source note | uspto-grants-2009_05 |
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