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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298354Generated: November 1, 2026

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

https://huagongshe.com/reaction/2298354

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

The product of Step 33a (6.1 g, 24 mmol) is dissolved in a mixture of THF, t-BuOH, 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 room temperature 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 1N NaOH and washed two times with ether. The aqueous solution is then acidified to pH<6 with concentrated HCl and a precipitate formed. The precipitate is collected by filtration and washed with 0.5M KHSO4 then water. The solid is dried in vacuo to give the product (5.7 g, 87%). MS for C11H7ClO2S2 (ESI) (M−H)− m/z 269.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492385B2
Source datasetuspto-grants-2002_12
ORD IDord-79b265130df04b68bfed859cedd4da7e
Source noteuspto-grants-2002_12