Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl 6-bromo-5-oxohexanoate | HCID 582216 | — |
| Reactant | HCID 22259560 | HCID 22259560 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 19877648 | HCID 19877648 | — |
Reaction Steps
Into 205 ml (1.16 mmol) of 6-hydroxynaphthalene-2-thiol was charged 5 ml of pyridine, and the mixture was stirred under an ice bath. A solution of 315 mg of methyl 6-bromo-5-oxohexanoate in 2 ml of pyridine was added, and the mixture was stirred under an ice bath for 1 hour. Further, the reaction was carried out at room temperature for 4 hours, by heating to 90° C. for 4 hours, and subsequently stirring was continued at room temperature overnight. The reaction mixture was neutralized with dilute hydrochloric acid and extracted with ethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05149859 |
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| Source dataset | uspto-grants-1992_09 |
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| ORD ID | ord-fd9f3472bd424ce0a4512f593af54332 |
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| Source note | uspto-grants-1992_09 |
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