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Ammonium Chloride → (7-Chloro-1,3-dioxaindan-5-yl)methanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | 7-Chloro-1,3-dioxaindane-5-carbaldehyde | HCID 676492 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (7-Chloro-1,3-dioxaindan-5-yl)methanol | HCID 4962440 | — |
反応手順
To a solution of 7-chlorobenzo[d][1,3]dioxole-5-carbaldehyde (6.0 g, 33 mmol) in THF (50 mL) was added NaBH4 (2.5 g, 64 mmol)) in portion at 0° C. The mixture was stirred at this temperature for 30 min and then poured into aqueous NH4Cl solution. The organic layer was separated, and the aqueous phase was extracted with EtOAc (50 mL×3). The combined extracts were dried over Na2SO4 and evaporated under reduced pressure to afford (7-chlorobenzo[d][1,3]dioxol-5-yl)methanol, which was directly used in the next step.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08846753B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-4aec2178fdcc41df98af1e562d44797c |
| 出典メモ | uspto-grants-2014_09 |