HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl acetate → Methyl 2-(tert-butoxy)-2-(2-methyl-1,3-thiazol-4-yl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl acetate | HCID 10908 | — |
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | Methyl 2-hydroxy-2-(2-methyl-1,3-thiazol-4-yl)acetate | HCID 86717830 | — |
| Product | Methyl 2-(tert-butoxy)-2-(2-methyl-1,3-thiazol-4-yl)acetate | HCID 70819407 | 21% |
Reaction Steps
Under a nitrogen atmosphere, perchloric acid (70%, 3.75 mL) was added at −10° C. to a solution of methyl 2-hydroxy-2-(2-methyl-1,3-thiazol-4-yl)acetate (15b) (590 mg, 3.15 mmol) in tertbutyl acetate (25 mL). After 1 hour, the reaction was quenched with a saturated aqueous solution of sodium carbonate and extracted with dichloromethane (2×20 mL). The organic layer was washed with brine (10 mL), dried over sodium sulfate, filtered and evaporated under reduced pressure. The residue was purified by flash chromatography on silica gel (dichloromethane/ethyl acetate 75/25) to afford the desired product (15c) as a white solid (160 mg, 0.66 mmol, 21%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238026B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-a0155373042d468ebceb1c08439e8652 |
| Source note | uspto-grants-2016_01 |