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Hydrochloric Acid → tert-Butyl 3-sulfanylpiperidine-1-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Sodium Methoxide | HCID 10942334 | — |
| 反応物 | 3-Acetylsulfanyl-1-Boc-piperidine | HCID 54776238 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | tert-Butyl 3-sulfanylpiperidine-1-carboxylate | HCID 49759132 | 101.4% |
反応手順
200 g of N-BOC-3(R,S)-acetylthio-piperidine are placed in a 10 l reactor with 3.4 l of methanol in an inert atmosphere. To this solution 42 g of sodium methoxide in methanol is added over a period of 15 min. After additional stirring 170 ml of 5 n HCl are added, bringing the pH-value to 2.6-3. The solution is concentrated at an evaporator. The resulting biphasic mixture is taken up with 1.7 l of methyl tert.-butyl ether (MTBE) and 1.7 l of water. After shaking, separation of the aqueous phase and washing the MTBE phase is isolated and evaporated, yielding 170 g of an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08334389B2 |
| 出典データセット | uspto-grants-2012_12 |
| ORD ID | ord-72c3b2e5c946452aa4f9613c5a2c80e9 |
| 出典メモ | uspto-grants-2012_12 |