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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412007Generated: October 26, 2026

2-Methyl-2-butene → 5-(4-Chlorophenylthio)thiophene-2-carboxylic acid

https://huagongshe.com/reaction/412007

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methyl-2-buteneHCID 10553—
ReactantPotassium bisulfateHCID 516920—
ReactantMonobasic potassium phosphateHCID 516951—
Reactant5-[(4-Chlorophenyl)sulfanyl]-2-thiophenecarbaldehydeHCID 7062194—
ReactantSodium ChloriteHCID 23668197—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
SolventTetrahydrofuranHCID 8028—
Product5-(4-Chlorophenylthio)thiophene-2-carboxylic acidHCID 2235040287.7%

Reaction Steps

5-(4-Chlorophenylsulfanyl)thiophene-2-carboxaldehyde (6.1 g, 24 mmol) is dissolved in a mixture of THF, tBuOH, and water (3:3:1, 255 mL). 2-methyl-2-butene (20.3 mL, 192 mmol) is added followed by KH2PO4 (9.8 g, 72 mmol) and then NaClO2 (80%, 8.17 g, 72.3 mmol). The mixture is stirred at rt for 2 hours. Aqueous KHSO4 (0.5M, 200 mL) is added and the organic solvents are removed in vacuo to produce an aqueous suspension of the product. The precipitate is collected by filtration, dissolved in IN NaOH and washed two times with ether. The aqueous solution is then acidified to pH<2 with concentrated HCl and a precipitate formed. The precipitate is collected by filtration and washed with 0.5M NaHSO4 then water. The solid is dried in vacuo to give 5.7 g (87%) of 5-(4-chlorophenylsulfanyl)thiophene-2-carboxylic acid. MS for C11H7ClO2S2, (ES) m/z: 269 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562816B2
Source datasetuspto-grants-2003_05
ORD IDord-291cb619609d471896591303a306e1b1
Source noteuspto-grants-2003_05