HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Methyl 2-(2-bromo-5-phenylthiophen-3-yl)-2-(tert-butoxy)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | Methyl 2-(2-bromo-5-phenylthiophen-3-yl)-2-hydroxyacetate | HCID 70818099 | — |
| Solvent | tert-Butyl acetate | HCID 10908 | — |
| Product | Methyl 2-(2-bromo-5-phenylthiophen-3-yl)-2-(tert-butoxy)acetate | HCID 70819299 | 173.9% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Methyl 2-(2-bromo-5-phenylthiophen-3-yl)-2-hydroxyacetate (11h) (75 mg, 0.23 mmol) was dissolved in tert-butyl acetate (8.6 mL) at 0° C. and 70% perchloric acid (1.1 mL) was rapidly added. The mixture was stirred at 0° C. for 30 minutes then poured in a saturated solution of potassium carbonate. Layers were separated. The aqueous layer was extracted with ethyl acetate (2×15 mL). The organic layers were washed with brine (8 mL), dried over sodium sulfate and concentrated in vacuo to provide the desired product (11i) (77 mg, 0.20 mmol, 87%) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238026B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-e0924bf67ed6436db3850b3eeff8de43 |
| Source note | uspto-grants-2016_01 |