関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N-Hydroxyphthalimide | HCID 10665 | — |
| 反応物 | Triphenylphosphine | HCID 11776 | — |
| 反応物 | 1-(Diphenylmethyl)azetidin-3-ol | HCID 330448 | — |
| 反応物 | Diethyl azodicarboxylate | HCID 5462977 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-{[1-(Diphenylmethyl)azetidin-3-yl]oxy}-1H-isoindole-1,3(2H)-dione | HCID 68338024 | 37.3% |
反応手順
To a solution of N-benzhydrylazetidin-3-ol (1.0 g, 4.18 mmol) in anhydrous THF (66 mL) under nitrogen were added N-hydroxyphthalimide (750 mg, 4.60 mmol) and triphenylphosphine (2.19 g, 8.36 mmol). The reaction mixture was cooled to 0° C. and DEAD (1.52 mL, 8.36 mmol) was added dropwise. The solution was allowed to warm to room temperature and stirred overnight. The reaction mixture was concentrated under reduced. The residue was purified on column chromatography (eluent: pentane/EtOAc 7/3 to 4/6) to give the title compound (600 mg, 37%) as a wax.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09051321B2 |
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| 出典データセット | uspto-grants-2015_06 |
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| ORD ID | ord-d0a31ed623b44b9582b5a1c6d06ff3fe |
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| 出典メモ | uspto-grants-2015_06 |
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