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Acetic Anhydride → (1-Acetyl-4-phenylpyrrolidin-3-yl)methanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | Methyl Cinnamate | HCID 637520 | — |
| 反応物 | 3-({[Tert-butyl(dimethyl)silyl]oxy}methyl)-4-phenylpyrrolidine | HCID 21912800 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | (1-Acetyl-4-phenylpyrrolidin-3-yl)methanol | HCID 68915138 | — |
反応手順
A pyridine solution of 3-({[tert-butyl(dimethyl)silyl]oxy}methyl)-4-phenylpyrrolidine which had been synthesized from methyl trans-cinnamate, in accordance with the technique of Ling et al. (“Tetrahedron”, 2001, vol. 57,p. 6579-6588) and the method of International Patent Publication WO 2000/59502, was mixed with acetic anhydride and stirred at room temperature for 2Hours. After completion of the reaction, this was concentrated under a reduced pressure with toluene azeotropy, and THF and 1 M THF solution of TBAF were added to the thus obtained residue and stirred overnight at room temperature. Thereafter, its work-up and purification were carried out in the standard method to obtain (1-acetyl-4-phenylpyrrolidin-3-yl)methanol. EP: 220.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07585886B2 |
| 出典データセット | uspto-grants-2009_09 |
| ORD ID | ord-5ed27cc94cc34c569d450626b02f55b1 |
| 出典メモ | uspto-grants-2009_09 |