Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Benzo[b]thiophene-6-carbonitrile | HCID 21816574 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzo[b]thiophen-6-ylmethanamine | HCID 54322319 | 82% |
Reaction Steps
Benzo[b]thiophene-6-carbonitrile (9.70 g, 61.1 mmol) is dissolved in THF (400 mL) and cooled to 0-5° C. Lithium aluminum hydride (183 mL of 1.0 M solution in THF) is added dropwise over 30 minutes and the reaction is stirred for 20 hours while warming to 25° C. The reaction is cooled with an ice bath and water (6.94 mL) is slowly added followed by 15% sodium hydroxide (6.94 mL) and water (20.83 mL). The resulting precipitate is filtered and washed with diethyl ether. The filtrate is concentrated to give the title compound as a colorless oil (8.16 g, 82% yield). ES+(m/z) 164 [M+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07547691B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-390d32111740437dab9bba2e3f55b663 |
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| Source note | uspto-grants-2009_06 |
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