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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300552Generated: October 30, 2026

Sulfuric Acid → Tert-butyl 5-bromothiophene-2-carboxylate

https://huagongshe.com/reaction/2300552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactanttert-ButanolHCID 6386—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant5-Bromothiophene-2-carboxylic acidHCID 349115—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 5-bromothiophene-2-carboxylateHCID 1091233594.4%

Reaction Steps

To a solution 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 16 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 of Step A (4.97 g). 1H NMR (400 MHz, CDCl3) δ 7.45 (d, 1H), 7.02 (d, 1H), 1.54 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498172B1
Source datasetuspto-grants-2002_12
ORD IDord-43c74a9ef01b429eb80829c2b933afc0
Source noteuspto-grants-2002_12