関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Trimethyl orthoformate | HCID 9005 | — |
| 反応物 | 9-Bromononanal | HCID 543330 | — |
| 触媒 | 1,4-Dioxane | HCID 31275 | — |
| 触媒 | Sodium Bicarbonate | HCID 516892 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 9-Bromo-1,1-dimethoxynonane | HCID 21880634 | 97.2% |
反応手順
To a 100 mL round-bottomed flask was added 9-bromononanal (7.2 g, 32.5 mmol), methanol (30 mL) and trimethylorthoformate (4 mL, 36.5 mmol). A solution of 4 N hydrochloric acid in dioxane (0.2 mL, 0.8 mmol) was added and the resulting mixture was refluxed for 3 h. The reaction mixture was then cooled to room temperature and solid sodium bicarbonate (100 mg, 1.2 mmol) was added. The resulting mixture was concentrated to one-fourth its original volume under reduced pressure and then ethyl acetate (50 mL) was added. The organic layer was washed with water (2×40 mL), dried (MgSO4), filtered and concentrated under reduced pressure to afford the title intermediate (8.44 g, (97% yield)) as a liquid, which as used in the next step without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07141671B2 |
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| 出典データセット | uspto-grants-2006_11 |
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| ORD ID | ord-44ac2e2617f24e7e816d83531a632205 |
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| 出典メモ | uspto-grants-2006_11 |
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