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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590986Generated: October 30, 2026

tert-Butyl acetate → Ethyl 2-(tert-butoxy)-2-(3,5-dibromothiophen-2-yl)acetate

https://huagongshe.com/reaction/590986

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl acetateHCID 10908—
ReactantPotassium CarbonateHCID 11430—
ReactantPerchloric AcidHCID 24247—
ReactantEthyl 2-(3,5-dibromothiophen-2-yl)-2-hydroxyacetateHCID 70818161—
ProductEthyl 2-(tert-butoxy)-2-(3,5-dibromothiophen-2-yl)acetateHCID 7081906886%

Reaction Conditions

Temperature0 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238026B2
Source datasetuspto-grants-2016_01
ORD IDord-90ecaf58ac954883ab8cdb2495c54294
Source noteuspto-grants-2016_01