HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl acetate → Ethyl 2-(tert-butoxy)-2-(3,5-dibromothiophen-2-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl acetate | HCID 10908 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | Ethyl 2-(3,5-dibromothiophen-2-yl)-2-hydroxyacetate | HCID 70818161 | — |
| Product | Ethyl 2-(tert-butoxy)-2-(3,5-dibromothiophen-2-yl)acetate | HCID 70819068 | 86% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Ethyl 2-(3,5-dibromothiophen-2-yl)-2-hydroxyacetate (10b) (160 mg, 0.47 mmol) was dissolved in tert-butyl acetate (8.7 mL) at −20° C. and 70% perchloric acid (1.1 mL) was rapidly added. The mixture was stirred at 0° C. for 3 hours then poured in a saturated solution of potassium carbonate. Layers were separated. The aqueous layer was extracted with ethyl acetate (2×20 mL). The organic layers were washed with brine (10 mL), dried over sodium sulfate and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 90/10) to provide the desired product (10c) (160 mg, 0.40 mmol, 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238026B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-90ecaf58ac954883ab8cdb2495c54294 |
| Source note | uspto-grants-2016_01 |