HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium Fluoride → 4-[((4-Carboxybutyl)[2-[2-([4-[2-(4-hydroxyphenyl)ethyl]benzyl]oxy)phenyl]-ethyl]amino)methyl]benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | Methyl 4-{[{2-[2-({4-[2-(4-{[tert-butyl(dimethyl)-silyl]oxy}phenyl)ethyl]benzyl}oxy)phenyl]ethyl}(5-ethoxy-5-oxopentyl)amino]-methyl}benzoate | HCID 23546389 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[((4-Carboxybutyl)[2-[2-([4-[2-(4-hydroxyphenyl)ethyl]benzyl]oxy)phenyl]-ethyl]amino)methyl]benzoic acid | HCID 23546266 | — |
Reaction Steps
27 mg (0.037 mmol) of methyl 4-{[{2-[2-({4-[2-(4-{[tert-butyl(dimethyl)-silyl]oxy}phenyl)ethyl]benzyl}oxy)phenyl]ethyl}(5-ethoxy-5-oxopentyl)amino]-methyl}benzoate from XXI are dissolved in 10 ml of THF. 0.03 ml of tetrabutylammonium fluoride (IM solution in THF) are added, and the solution is stirred at RT for 1 hour. The solvents are evaporated under reduced pressure. The residue is dissolved in 2 ml of methanol. 0.05 ml of aqueous sodium hydroxide solution, 45%, and 0.2 ml of dichloromethane are added, and the solution is stirred at RT for 8 hours. The mixture is concentrated, water is added and the solution is acidified using sulphuric acid. The solid is filtered off and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07087644B1 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-3350d545ae14418b8df6f55ce8d0020d |
| Source note | uspto-grants-2006_08 |