HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63617Generated: October 26, 2026
Trimethylsilyl cyanide → HCID 82623563, compound
https://huagongshe.com/reaction/63617
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 7-bromo-3,4-dihydro-2H-1-benzopyran-4-one | HCID 22335736 | — |
| Catalyst | zinc(II)iodide | HCID 9883512 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 82623563 | HCID 82623563 | 79.2% |
Reaction Steps
To a solution of 7-bromochroman-4-one (5.00 g, 22.0 mmol) and ZnI2 (30 mg) in toluene (50 mL) was added TMSCN (4.36 g, 44.0 mmol), and the mixture was heated at 60° C. overnight. The reaction mixture was cooled to rt, and a solution of LAH (20.0 mL, 2.4 M in THF, 44.0 mmol) was added slowly. The mixture was stirred at 40° C. for 2 h. The reaction was quenched with the addition of EtOAc (10 mL) at 0° C., followed by water (5 mL) and aqueous 10% NaOH (5 mL). The reaction mixture was diluted with EtOAc, dried (MgSO4), filtered through Celite, and concentrated to give 4.5 g (79%) of the crude 4-(aminomethyl)-7-bromo-3,4-dihydro-2H-1-benzopyran-4-ol intermediate as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09447046B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-0ac686a3c07b4d78994868ae452911bf |
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| Source note | uspto-grants-2016_09 |
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