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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | 2-Bromo-3-methylthiophene | HCID 84314 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 3-Methoxypropyl 4-methylbenzenesulfonate | HCID 13522988 | — |
| Catalyst | 2-Bromo-3-methylthiophene | HCID 84314 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(3-Methoxy-propyl)-3-methyl-thiophene | HCID 66856557 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07868030B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-ddb5c2e17f394f9c8d725315dd4ac8e4 |
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| Source note | uspto-grants-2011_01 |
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