HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480328Generated: October 26, 2026
Sulfuric Acid → Tert-butyl 5-bromothiophene-2-carboxylate
https://huagongshe.com/reaction/480328
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Sulfuric acid magnesium salt (1:1) | HCID 24083 | — |
| Reactant | 5-Bromothiophene-2-carboxylic acid | HCID 349115 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 5-bromothiophene-2-carboxylate | HCID 10912335 | 94.4% |
Reaction Steps
To a mixture of anhydrous MgSO4 (11.60 g, 96.4 mmol) in 100 mL CH2Cl2 was added concentrated H2SO4 (1.45 mL, 24.1 mmol) and the mixture was stirred for 15 minutes followed by addition of 5-bromo-thiophene-2-carboxylic acid (5.0 g, 24.1 mmol). After stirring for 1 minute, tert-butanol (11.6 g, 20 mmol) was added and the reaction was stirred at room temperature for 18 h. The reaction was quenched with saturated NaHCO3. The layers were separated, the aqueous layer was extracted with CH2Cl2, and the combined organic layers were dried over MgSO4. The organic solution was concentrated to give a clear oil which was purified via medium pressure chromatography (3% EtOAc in hexanes) to afford the title compound (4.97 g). 1H NMR (400 MHz, CDC13) δ 7.45 (d, 1H), 7.02 (d, 1H), 1.54 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06649657B2 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-ad92f0ef1cd84c899d778096ff0370f7 |
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| Source note | uspto-grants-2003_11 |
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