HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157963Generated: November 3, 2026
Trimethylsilyl cyanide → HCID 25232593, compound
https://huagongshe.com/reaction/1157963
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | 2-Fluoro-4,5-dimethoxybenzaldehyde | HCID 603595 | — |
| Reactant | Ytterbium triflate | HCID 2733225 | — |
| Reactant | HCID 25232416 | HCID 25232416 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 25232593 | HCID 25232593 | — |
Reaction Steps
To a mixture of Yb(OTf)3(0.399 g) and dichloromethane (25 mL) there were added (5-amino-2-bromobenzyl)carbamic acid t-butyl ester (Example (3a))(1.95 g), 2-fluoro-4,5-dimethoxybenzaldehyde (1.19 g), MS3A (2.58 g) and trimethylsilyl cyanide (1.29 mL) in that order under a nitrogen atmosphere, and the mixture was stirred at room temperature for 16 hours. The solvent in the mixture was distilled off under reduced pressure, ethyl acetate (200 mL) and water (100 mL) were added to the residue, and after sufficiently shaking the mixture, the organic layer was separated off, washed with saturated aqueous sodium chloride (100 mL) and dried over anhydrous magnesium sulfate. The mixture was filtered to obtain a filtrate, and the solvent in the filtrate was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate-heptane mixture) to obtain the target compound (2.98 g) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07807690B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-48fcc1b54b9e4942b45de7d1eb1f4183 |
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| Source note | uspto-grants-2010_10 |
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