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HRID 81743作成日:2026年10月26日
(1-Isopropyl-2-methyl-propyl)-(2,4,5-trimethoxy-benzylidene)-amine → (2-Isopropyl4,5-dimethoxy-benzylidene)-(1-isopropyl-2-methyl-propyl)-amine
https://huagongshe.com/reaction/81743
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | (1-Isopropyl-2-methyl-propyl)-(2,4,5-trimethoxy-benzylidene)-amine | HCID 59598598 | — |
| 反応物 | HCID 178506895 | HCID 178506895 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (2-Isopropyl4,5-dimethoxy-benzylidene)-(1-isopropyl-2-methyl-propyl)-amine | HCID 59598696 | — |
反応手順
To a solution of (1-isopropyl-2-methyl-propyl)-(2,4,5-trimethoxy-benzylidene)-amine (1.024 g, 3.5 mmol) in 35 ml THF at −78° C. was added isopropyllithium (6.0 mL, 0.7 M in pentane) drop-wise over 5 minutes. The solution was allowed to stir 30 min at −78° C. After warming to room temperature over 45 minutes the mixture was quenched by the addition of 5 mL of 10% NH4Cl and concentrated in vacuo. 100 mL of H2O was added and the mixture was extracted with ethyl acetate, washed with H2O and then brine. The combined organic layers were dried over Na2SO4, filtered and concentrated in vacuo to give (2-isopropyl-4,5-dimethoxy-benzylidene)-(1-isopropyl-2-methyl-propyl)-amine as a yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08846705B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-b82b84a4f1c54be5b48023909d66cb54 |
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| 出典メモ | uspto-grants-2014_09 |
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