HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593307Generated: October 29, 2026
Allyl bromide → 2-Allyl-6-methoxy-tetralin-1-one
https://huagongshe.com/reaction/593307
Participants
| Role | Name | HCID | Charge |
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| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | 6-Methoxy-alpha-tetralone | HCID 14112 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Allyl-6-methoxy-tetralin-1-one | HCID 18794575 | 20.5% |
Reaction Steps
Allyl bromide (5.4 g, 45.0 mmol) was added to a solution of 6-methoxy-1-tetralone (10.0 g, 56.0 mmol) and potassium tert-butoxide in THF (50 mL), and the reaction mixture was stirred at room temperature for 18 h. The reaction mixture was then diluted with ethyl acetate. The separated organic layer was washed with water, brine solution, dried over sodium sulphate, filtered and removed under reduced pressure. The product was purified by flash chromatography using 4% ethyl acetate in hexanes to afford title compound (2.0 g, 15%) as solid. 1H NMR (400 MHz, CDCl3): δ 8.01 (d, J=8.4 Hz, 1H), 6.80 (dd, J1=2.8 Hz, J2=8.8 Hz, 1H), 6.68 (m, 1H), 5.89-5.79 (m, 1H), 5.12 (t, J=17.2 Hz, 2H) 3.85 (s, 3H), 2.95 (m, 2H), 2.93-2.72 (m, 1H), 2.53-2.46 (m, 1H), 2.29-2.17 (m, 2H), 1.89-1.79 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242929B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-bae04a9aa31549ef97b30b276408cab2 |
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| Source note | uspto-grants-2016_01 |
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