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4-Hydroxybenzaldehyde → 4-[[6-(Diethylamino)hexyl]oxy]benzaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Hydroxybenzaldehyde | HCID 126 | — |
| 反応物 | Triphenylphosphine | HCID 11776 | — |
| 反応物 | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| 反応物 | 6-(Diethylamino)-1-hexanol | HCID 245054 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 4-[[6-(Diethylamino)hexyl]oxy]benzaldehyde | HCID 19761013 | 64.3% |
反応手順
A mixture of 2.17 g of 6-diethylamino-1-hexanol (J. Chem. Soc. 1942, 428), 1.52 g of 4-hydroxy-benzaldehyde and 3.3 g of triphenylphosphine in 100 ml of tetrahydrofuran was treated slowly at 20° with a solution of 1.97 g of diethyl azodicarboxylate. After the dropwise addition the mixture was stirred at room temperature for a further 5 hours. The reaction mixture was then evaporated in a rotary evaporator. The residue was chromatographed on 400 g of neutral aluminium oxide (activity grade III) with hexane:ethyl acetate (7:3). There were obtained 2.22 g (64%) of 4-[[6-(diethylamino)hexyl]oxy]benzaldehyde as a yellowish oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05214046 |
| 出典データセット | uspto-grants-1993_05 |
| ORD ID | ord-187ac58ef0194af39d7fd19eefd6b4ef |
| 出典メモ | uspto-grants-1993_05 |