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Hydrochloric Acid → Diethyl 2-(3-(2,6-dimethylbenzyloxy)benzoyl)pentanedioate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Ethyl 3-bromopropionate | HCID 68320 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 反応物 | Ethyl 3-(3-(2,6-dimethylbenzyloxy)phenyl)-3-oxopropanoate | HCID 66875194 | — |
| 溶媒 | tert-Butanol | HCID 6386 | — |
| 生成物 | Diethyl 2-(3-(2,6-dimethylbenzyloxy)benzoyl)pentanedioate | HCID 66875332 | — |
反応手順
To a solution of Ethyl 3-(3-(2,6-dimethylbenzyloxy)phenyl)-3-oxopropanoate (Step A, 5 g, 16.02 mmol) in t-butyl alcohol (50 ml) was added a solution of potassium tert-butoxide (1M in t-butyl alcohol, 1.988 g, 17.7 mmol) and the reaction mixture was stirred for 30 minutes at room temperature. Ethyl 3-bromopropionate was added drop wise to the reaction mixture and stirring continued for another 2 hours and then poured into 1M HCl, extracted with ethyl acetate (2×), washed with brine, dried over Na2SO4, filtered, concentrated and purified by flash chromatography eluted with hexane:ethyl acetate (2:1) to give the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08829058B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-8731ede7ec354442beb9aed4ad52a959 |
| 出典メモ | uspto-grants-2014_09 |