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Dimethylformamide → Tert-butyl {4-[2-(benzyloxy)-2-oxoethyl]phenoxy}acetate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | tert-Butyl bromoacetate | HCID 79177 | — |
| 反応物 | Benzyl 2-(4-hydroxyphenyl)acetate | HCID 11107524 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | Tert-butyl {4-[2-(benzyloxy)-2-oxoethyl]phenoxy}acetate | HCID 68357704 | 98.3% |
反応手順
Potassium carbonate (1.38 g) and tert-butyl bromoacetate (1.07 g) were added to a dehydrated N,N-dimethylformamide (17 mL) solution of benzyl (4-hydroxyphenyl)acetate (1.21 g) at room temperature, followed by stirring for 1 hour. Thereafter, water was added to the reaction mixture on an ice bath, and extraction was performed with hexane:ethyl acetate=2:1. The resulting organic phase was washed with an aqueous saturated sodium chloride solution and dried with anhydrous sodium sulfate, followed by concentration under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1→8:2) to obtain the title compound (1.75 g) having the following physical property values.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09353113B2 |
| 出典データセット | uspto-grants-2016_05 |
| ORD ID | ord-4bb030380e974bc88169e9b0d50458a6 |
| 出典メモ | uspto-grants-2016_05 |