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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252268Generated: October 26, 2026

Hydrochloric Acid → 2-(3-Methoxy-propyl)-3-methyl-thiophene

https://huagongshe.com/reaction/252268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIodineHCID 807—
Reactant2-Bromo-3-methylthiopheneHCID 84314—
ReactantMagnesiumHCID 5462224—
Reactant3-Methoxypropyl 4-methylbenzenesulfonateHCID 13522988—
Catalyst2-Bromo-3-methylthiopheneHCID 84314—
SolventDiethyl EtherHCID 3283—
Product2-(3-Methoxy-propyl)-3-methyl-thiopheneHCID 66856557—

Reaction Conditions

Temperature30 °C

Reaction Steps

Magnesium turnings (365 mg, 15.0 mmol, 1.5 equiv.) were suspended in 15 ml dry diethyl ether. A crystal of iodine and a few drops of 2-bromo-3-methylthiophene in 10 ml ether were added till the reaction started (3 min. with heating to 30° C.). The remaining solution of 2-bromo-3-methylthiophene (total 2.44 g, 10.0 mmol, 1.0 equiv.) was added dropwise to maintain the reaction at reflux. The reaction mixture was refluxed for 30 min. Toluene-4-sulfonic acid 3-methoxy-propyl ester (2.13 g, 12.0 mmol, 1.2 equiv.) dissolved in 5 ml diethyl ether was added dropwise and the yellow solution was refluxed again for 2 hours. The brown suspension was cooled, acidified with 1N HCl and extracted twice with ethyl acetate. The combined organics were washed with KHSO4/K2SO4 and brine, dried over Na2SO4, filtered, evaporated and chromatographed on a 50 g Silicagel cartridge with heptane and than MTBE-heptane 1:9 as solvent to give 2-(3-methoxy-propyl)-3-methyl-thiophene, 410 mg, m/e 170.0 (MH+) by GC/MS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868030B2
Source datasetuspto-grants-2011_01
ORD IDord-ddb5c2e17f394f9c8d725315dd4ac8e4
Source noteuspto-grants-2011_01