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Tetrahydrofuran → 1-(t-Butoxycarbonylmethoxyphenyl)-3,5-di(4-hydroxyphenyl)benzene
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | 1,3,5-Tris(4-hydroxyphenyl)benzene | HCID 348148 | — |
| 反応物 | Bromo-t-butylacetate | HCID 21584499 | — |
| 反応物 | Potassium tert-butoxide | HCID 23665647 | — |
| 生成物 | 1-(t-Butoxycarbonylmethoxyphenyl)-3,5-di(4-hydroxyphenyl)benzene | HCID 68862158 | — |
反応手順
18 g of 1,3,5-tris(4-hydroxyphenyl)benzene was dissolved in 500 ml of tetrahydrofuran. 6 g of potassium t-butoxide was added and the mixture was stirred at room temperature for five minutes. After the addition of 10 g of bromo-t-butylacetate dropwise, the mixture was stirred for six hours while heating at 60° C. After evaporating tetrahydrofuran under reduced-pressure, the reaction product was extracted with 300 ml of dichloromethane, purified using a silica gel column, and dried to obtain 4.6 g of 1-(t-butoxycarbonylmethoxyphenyl)-3,5-di(4-hydroxyphenyl)benzene.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08361691B2 |
| 出典データセット | uspto-grants-2013_01 |
| ORD ID | ord-465366b4c54a446ba9b337ebada64dcf |
| 出典メモ | uspto-grants-2013_01 |