HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 1-(t-Butoxycarbonylmethoxyphenyl)-3,5-di(4-hydroxyphenyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1,3,5-Tris(4-hydroxyphenyl)benzene | HCID 348148 | — |
| Reactant | Bromo-t-butylacetate | HCID 21584499 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Product | 1-(t-Butoxycarbonylmethoxyphenyl)-3,5-di(4-hydroxyphenyl)benzene | HCID 68862158 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08361691B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-465366b4c54a446ba9b337ebada64dcf |
| Source note | uspto-grants-2013_01 |