Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22620529 | HCID 22620529 | — |
| Product | HCID 22620483 | HCID 22620483 | — |
Reaction Steps
6-[Bis(methylthio)methylene]-9-ethyl-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-one (0.35 g, 1.31 mmol) was dissolved in ethanol (7 ml), followed by adding thereto sodium tetrahydroborate (0.16 g, 4.35 mmol), and the reaction mixture was heated under reflux for 2 hours. The reaction mixture was poured into ice water and extracted with ethyl acetate, and the extract solution was washed with a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and boron trifluoride diethyl ether complex (0.56 g, 3.95 mmol) was added to the residue, followed by stirring at room temperature for 20 minutes. Then, methanol (5 ml) was added thereto and the resulting mixture was heated under reflux for 3 hours. The reaction mixture was poured into ice water and extracted with ethyl acetate, and the extract solution was washed with a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was purified by a silica gel column chromatography to obtain 0.20 g of methyl 5-ethyl-6,7-dihydro-5H-benzocycloheptene-8-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06369110B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-dc0b97c8f97c4bce92f414fe45c251df |
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| Source note | uspto-grants-2002_04 |
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