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HRID 505704作成日:2026年10月26日
Pyrrolidine → (+/-)-Methyl 5-oxo-6-((tetrahydrofuran-3-yl)methylene)-5,6,7,8-tetrahydronaphthalene-2-carboxylate
https://huagongshe.com/reaction/505704
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Pyrrolidine | HCID 31268 | — |
| 反応物 | 3-Furancarboxaldehyde, tetrahydro- | HCID 157568 | — |
| 反応物 | Methyl 5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylate | HCID 15309116 | — |
| 反応物 | Ethyl acetate hexane | HCID 21226206 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | (+/-)-Methyl 5-oxo-6-((tetrahydrofuran-3-yl)methylene)-5,6,7,8-tetrahydronaphthalene-2-carboxylate | HCID 66723025 | 58.2% |
反応手順
To a solution of methyl 5-oxo-5,6,7,8-tetrahydronaphthalene-2-carboxylate (240 mg, 1.2 mmol) in methanol (3 mL) was added (±)-tetrahydrofuran-3-carboxaldehyde (240 mg, 2.4 mmol) and pyrrolidine (0.20 mL, 2.4 mmol). The solution was stirred for twenty hours at ambient temperature and for four hours at 45° C. The reaction was concentrated in vacuo. Chromatography (on silica, ethyl acetate/hexane) provided (±)-methyl 5-oxo-6-((tetrahydrofuran-3-yl)methylene)-5,6,7,8-tetrahydronaphthalene-2-carboxylate as an orange oil (200 mg, 58% yield). LC/MS on 4.6×50 mm C-18 column, tR=2.52 minutes (10 to 90% acetonitrile/water over 4 minutes at 4 mL/minute with detection 254 nm, at 50° C.); ES-MS m/z 287 (M+H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07781428B2 |
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| 出典データセット | uspto-grants-2010_08 |
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| ORD ID | ord-2f266235f3e641049e3a9e320e8f7cf7 |
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| 出典メモ | uspto-grants-2010_08 |
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