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Hexamethylenetetramine → 2-Hydroxy-4-chloro-5-(1,1-dimethylethyl)benzaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hexamethylenetetramine | HCID 4101 | — |
| 反応物 | Trifluoroacetic acid | HCID 6422 | — |
| 反応物 | 4-tert-Butyl-3-chlorophenol | HCID 13499472 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2-Hydroxy-4-chloro-5-(1,1-dimethylethyl)benzaldehyde | HCID 23035427 | 17% |
反応手順
A mixture of 9.65 g (52.2 mmol) of 3-chloro-4-(1,1-dimethylethyl)phenol and 7.37 g (52.2 mmol) of hexamethylenetetramine was refluxed in 150 ml of trifluoroacetic acid for 3 hours. The solution was cooled to ambient temperature and diluted with 500 ml of water. The aqueous residue was extracted with ether. The organic phase was washed with saturated sodium bicarbonate solution, dried and evaporated. The residue was chromatographed on 250 g of silica gel using a gradient from hexane to 20:80 (v/v) ether: hexane as eluent. There was obtained 1.87 g (8.79 mmol, 17%) of 2-hydroxy-4-chloro-5-(1,1-dimethylethyl)benzaldehyde; mp 38°-39° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04952583 |
| 出典データセット | uspto-grants-1990_08 |
| ORD ID | ord-375129a6d5c34d1b9ba00aca701d145e |
| 出典メモ | uspto-grants-1990_08 |