HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099036Generated: October 26, 2026
Water → 2-[4-(1-Methyl-hexyloxy)-phenyl]-thiophene
https://huagongshe.com/reaction/2099036
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 2-(Tri-n-butylstannyl)thiophene | HCID 2779373 | — |
| Reactant | 1-Bromo-4-(1-methyl-hexyloxy)-benzene | HCID 20096785 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[4-(1-Methyl-hexyloxy)-phenyl]-thiophene | HCID 57562023 | 44.4% |
Reaction Steps
Tetrakistriphenylphosphinpalladium(0), (20.45 g, 17.70 mmol) is suspended in anhydrous DMF (400 mL) in a 2000 mL 3-necked flask with magnetic stirrer and condenser under an argon atmosphere. To this, 1-bromo-4-(1-methyl-hexyloxy)-benzene (240.00 g, 884.96 mmol) and tri-n-butylstannylthiophene (330.24 g, 884.96 mmol) are added. The resulting solution is stirred at 100° C. for 68 hours. After cooling to room temperature the mixture is poured into water (2000 mL) and divided into two portions of the same volume. Extraction with n-hexane (3×300 mL) results in two layers and an emulsion between those two layers. The organic layers are separated, combined, washed with diluted sodium chloride solution (2×400 mL) and dried (MgSO4). After removal of solvent by rotary evaporation most of the byproducts are removed by distillation (p=10−3 millibar, maximum temperature Tmax=130° C.). The residue is subjected to filtration using a layer of SiO2 (30×10 cm) and n-hexane as eluent. After removal of solvent, a yellowish oil (107.88 g, about 44%) with sufficient purity for synthetic purposes is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07569415B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-b9ad81e7c1634bbd9fa1564a3fbc9ecd |
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| Source note | uspto-grants-2009_08 |
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