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5-Cyano-2-furaldehyde → 5-(Hydroxymethyl)furan-2-carbonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 5-Cyano-2-furaldehyde | HCID 642139 | — |
| 反応物 | Potassium borohydride | HCID 4192641 | — |
| 反応物 | Monosodium phosphate | HCID 23672064 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 5-(Hydroxymethyl)furan-2-carbonitrile | HCID 3021406 | 87.1% |
反応手順
0.87 g of the aldehyde of Stage A in 5 ml of tetrahydrofuran and 1 ml of water was cooled to 0° C. and 0.47 g of potassium borohydride were introduced. The mixture was stirred for 5 hours, poured into an aqueous sodium dihydrogenphosphate solution and extracted with isopropyl ether. The extract was dried and the solvent was evaporated to obtain 0.77 g of the expected product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05405865 |
| 出典データセット | uspto-grants-1995_04 |
| ORD ID | ord-5e604ca6abc64148b01f7f7b4b997bd6 |
| 出典メモ | uspto-grants-1995_04 |