HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2235641Generated: October 30, 2026
Potassium Carbonate → (5-(4-Butylphenyl)thiophen-2-yl)methanol
https://huagongshe.com/reaction/2235641
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Butylphenylboronic acid | HCID 4100860 | — |
| Reactant | (5-Bromothiophen-2-yl)methanol | HCID 11435467 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (5-(4-Butylphenyl)thiophen-2-yl)methanol | HCID 59300633 | 19% |
Reaction Steps
A mixture of 60.2 (0.300 g, 1.55 mmol), 4-n-butylbenzeneboronic acid 60.3 (0.553 g, 3.11 mmol), K2CO3 (0.644 g, 4.66 mmol), and Pd(PPh3)4 (0.180 g, 0.16 mmol) in toluene (5 mL) was stirred overnight at 95° C. The mixture was cooled to room temperature, filtered through a pad of silica gel (EtOAc), and concentrated. The crude product was chromatographed on silica gel (0-40% EtOAc/hexane) to afford 60.4 (0.072 g, 19%). 1H NMR (400 MHz, CDCl3) δ 7.49 (d, 2H), 7.18 (d, 2H), 7.13 (d, 1H), 6.97 (d, H), 4.82 (s, 2H), 2.62 (t, 2H), 1.60 (m, 2H), 1.37 (m, 2H),
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07714008B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-c480bb00da3a400087081671476731ac |
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| Source note | uspto-grants-2010_05 |
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