HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121297Generated: November 1, 2026
Dichloromethane → 2-(4-Hydroxyphenyl)-5-pentylthiophene
https://huagongshe.com/reaction/2121297
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 2-(4-Methoxyphenyl)-5-pentylthiophene | HCID 23432113 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(4-Hydroxyphenyl)-5-pentylthiophene | HCID 23432314 | 81.4% |
Reaction Steps
A solution of boron tribromide (3.2 cm3) and dichloromethane (30 cm3) was added dropwise to a solution of 2-(4-methoxyphenyl)-5-pentylthiophene (10.0 g) and dichloromethane (70 cm3) at 0° C. under an atmosphere of nitrogen. The reaction solution was stirred overnight at room temperature and water (100 cm3) added. The organic layer was separated off and the aqueous layer extracted with dichloromethane (2×100 cm3). The combined organic layers were washed with brine (2×100 cm3) and then dried (MgSO4), filtered and evaporated down. The residue was purified by column chromatography on silica gel using a 4:1 hexane/dichloromethane mixture as eluent and recrystallisation from hexane to yield 7.7 g of g 2-(4-hydroxyphenyl)-5-pentylthiophene, K 100-102° C., I.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06696110B1 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-16905664bdd644e98b28daabbe53758f |
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| Source note | uspto-grants-2004_02 |
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