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Hydrochloric Acid → N-Benzyl-N-(trimethylsilylmethyl)aminoacetonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Formaldehyde | HCID 712 | — |
| 反応物 | Potassium Cyanide | HCID 9032 | — |
| 反応物 | N-[(Trimethylsilyl)methyl]benzylamine | HCID 353458 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | N-Benzyl-N-(trimethylsilylmethyl)aminoacetonitrile | HCID 560960 | 100.5% |
反応手順
Part B 1 N Hydrochloric acid solution (119 mL) was added to N-benzyl-N-trimethylsilanylmethyl-amine (23.00 g, 119 mmol) and white precipitate formed. Tetrahydrofuran (650 mL), potassium cyanide (9.3 g, 143 mmol), and aqueous formaldehyde solution (37 wt. %, 12 mL, 155 mmol) were added to the reaction mixture and stirred at ambient temperature for 15 hours. The mixture was extracted with ether and separated and the combined organic layers were washed with water, dried over magnesium sulfate, and concentrated sequentially under reduced pressure and high vacuum at ambient temperature to afford 27.80 g of (N-Benzyl-N-trimethylsilanylmethyl-amino)acetonitrile. Part C
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07544697B2 |
| 出典データセット | uspto-grants-2009_06 |
| ORD ID | ord-115eeeff47644468b59861dc4c7f0d06 |
| 出典メモ | uspto-grants-2009_06 |