HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387689Generated: October 25, 2026
Triphenylphosphine → 4-(3-Chloropropyl)pyridine
https://huagongshe.com/reaction/387689
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 4-Pyridinepropanol | HCID 72923 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(3-Chloropropyl)pyridine | HCID 205442 | 78.8% |
Reaction Steps
3-(4-Pyridyl)-1-propanol (2.68 g, 19.3724 mmol) was dissolved in dichloromethane (100 ml), triphenylphosphine (5.6 g. 21.3096 mmol) was added, and then N-chlorosuccinimide (2.6 g, 19.3724 mmol) was gradually added while cooling on ice prior to stirring overnight. After distilling off the solvent under reduced pressure, the residue was dissolved in ethyl acetate and extracted with 1N hydrochloric acid. Upon neutralization with saturated bicarbonate water, the mixture was extracted with ethyl acetate, washed with saturated saline and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure to obtain the title compound (2,375 g, 15.2605 mmol, 78.77%) as a yellowish-brown oil. This was used without further purification for the following reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372981B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-e5e88d60add44403b3c171510992fffb |
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| Source note | uspto-grants-2013_02 |
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