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p-Toluenesulfonic acid → HCID 178491344、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | 3-Pentanamine, 2,4-dimethyl- | HCID 77702 | — |
| 反応物 | 2,6-Dimethoxybenzaldehyde | HCID 96404 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | HCID 178491344 | HCID 178491344 | — |
反応手順
A mixture of 25.0 g (150 mmol) 2,6-dimethoxybenzaldehyde, 19.1 g (165 mmol) 3-amino-2,4-dimethylpentane and 0.500 g p-toluenesulfonic acid in 100 ml toluene was heated in a Dean-Stark apparatus to reflux for 2 hours. Then the cooled reaction mixture was washed with aqueous NaHCO3 solution, brine dried over Na2SO4, filtered and evaporated. The crude product was filtered through a silica pad with heptane/ethyl acetate 2:1 as eluent: 22.0 g [1-(2,6-dimethoxy-phenyl)-meth-(E)-ylidene]-(1-isopropyl-2-methyl-propyl)-amine as slightly yellow crystals: MS (EI): 264.3 ((M+H)+.), 262.3 ((M-H)+.), 248.3 ((M−CH3)+.), 220.2 ((M−(CH3)2CH)+.), 100%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07875645B2 |
| 出典データセット | uspto-grants-2011_01 |
| ORD ID | ord-d89bcb139b314bc49a6166f783772c3f |
| 出典メモ | uspto-grants-2011_01 |