HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458595Generated: October 29, 2026
Pyridine → 4-(4-Methoxyphenyl)butyl 4-methylbenzene-1-sulfonate
https://huagongshe.com/reaction/458595
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 4-(4-Methoxyphenyl)butan-1-ol | HCID 97660 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-(4-Methoxyphenyl)butyl 4-methylbenzene-1-sulfonate | HCID 11045901 | 70.1% |
Reaction Steps
Pyridine (15 mL) was added drop wise to a cooled (0° C.) solution of 4-(4-methoxyphenyl)butanol (10.0 g, 0.055 mol) and p-toluenesulfonyl chloride (13.6 g, 0.072 mol) in dry chloroform (100 mL) under stirring. The reaction mixture was stirred overnight at room temperature. After this time, the reaction was quenched with 10% HCl (300 mL) and extracted with chloroform. The organic fraction was washed with saturated NaHCO3, water and dried over magnesium sulfate. The solvent was removed under reduced pressure and the residue purified by flash chromatography (eluent:hexane/ethyl acetate 15:1) to provide 12.9 g (66%) of 1 as clear oil. 1H NMR (360 MHz, CDCl3) δ 1.61 (m, 4H), 2.44 (s, 3H), 2.52 (m, 2H), 3.78 (s, 3H), 4.05 (m, 2H), 6.77 (d, 2H), 7.05 (d, 2H), 7.34 (d, 2H), 7.78 (d, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192959B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-7dcbdc5d534e4871a9a5bf92c1c977b9 |
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| Source note | uspto-grants-2007_03 |
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