Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Salicylate | HCID 4133 | — |
| Reactant | 2-Bromomethylnaphthalene | HCID 70320 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21190790 | HCID 21190790 | 88% |
Reaction Steps
3.9 g (35 mmol) of potassium tert-butoxide were added a little at a time to 5 g (33 mmol) of methyl hydroxybenzoate in 200 ml of dimethylformamide. After about 15 min, a further 7.3 g (33 mmol) of 2-(bromomethyl)naphthalene were added and the reaction mixture was heated to 100° C. for about 3 h. The reaction mixture was then poured into ice-water and the product was extracted with ethyl acetate. The organic phase was dried and concentrated under reduced pressure. 8.4 g (88%) of the product were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06251917B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-833350f76b0d45298dfe49e0745dfc35 |
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| Source note | uspto-grants-2001_06 |
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