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Trifluoroacetic acid → N-benzyloxy-N-(2-methylpropyl)amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Trifluoroacetic acid | HCID 6422 | — |
| 反応物 | tert-butyl N-benzyloxy-N-(2-methylpropyl)carbamate | HCID 19967428 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-benzyloxy-N-(2-methylpropyl)amine | HCID 19967392 | 101.2% |
反応手順
Trifluoroacetic acid (21 mL, 270 mmol) was added in a single portion to a solution of tert-butyl N-benzyloxy-N-(2-methylpropyl)carbamate (7.6 g, 27 mmol) in methylene chloride (21 mL). A spontaneous reflux occurred. The reaction mixture was stirred without external heating for 20 minutes and then concentrated under vacuum at 45° C. Saturated aqueous sodium bicarbonate was added to the residue followed by a quantity of solid sodium bicarbonate sufficient to bring the pH of the reaction mixture up to a value of 9. The mixture was extracted twice with methylene chloride. The extracts were combined, dried over magnesium sulfate then concentrated under vacuum to provide 4.9 g of N-benzyloxy-N-(2-methylpropyl)amine as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05612377 |
| 出典データセット | uspto-grants-1997_03 |
| ORD ID | ord-dc8021c5fc3a41f08acdf0f7506a6e60 |
| 出典メモ | uspto-grants-1997_03 |