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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359635Generated: October 28, 2026

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

https://huagongshe.com/reaction/1359635

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. Ig, 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 numberUS06599916B2
Source datasetuspto-grants-2003_07
ORD IDord-fe6c173f6baf47e693ae2ddf0fdb0c4e
Source noteuspto-grants-2003_07