Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Methyl-2-thiophenecarboxaldehyde | HCID 79911 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 178418336 | HCID 178418336 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 19819833 | HCID 19819833 | — |
Reaction Steps
To a stirred solution of 50 g (0.40 mol) of 3-methyl-2-thiophenecarboxaldehyde in 150 ml of dry tetrahydrofuran at 0° C. was added dropwise 476 ml (0.47 mol) of a 1M solution of lithium bis(trimethylsilyl)amide in tetrahydrofuran over a 2 hour period. After stirring the mixture an additional 20 minutes at 0° C., 476 ml (0.47 mol) of a 1M solution of benzyl magnesium chloride in diethyl ether was added dropwise over a 2 hour period. The resulting mixture was allowed to warm to ambient temperature, stirred for 0.5 h longer, and poured into 2.5 L of saturated aqueous ammonium chloride. The mixture was extracted with chloroform (3×500 ml), organic layers combined, dried over MgSO4, and concentrated to dryness giving 85 g of the title amine as an oil. A sample of the product (4 g) was dissolved in isopropanol, made acidic with hydrogen chloride in isopropanol, decolorized with carbon, and reconcentrated to near dryness. The crude hydrochloride salt was recrystallized from a solvent mixture of ethyl acetate and methanol to give 2.5 g of white solid (mp 184°-186° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05109017 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-1dd76c4f9667436da9fe946a0dd24ae8 |
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| Source note | uspto-grants-1992_04 |
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