HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253497Generated: November 1, 2026
Thionyl Chloride → 1-Benzyl-2-(chloromethyl)pyrrolidine
https://huagongshe.com/reaction/1253497
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (1-Benzylpyrrolidin-2-yl)methanol | HCID 562951 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-Benzyl-2-(chloromethyl)pyrrolidine | HCID 3042642 | — |
Reaction Steps
Into a 5,000 ml 3-necked roundbottom flask, was placed a solution of (1-benzylpyrrolidin-2-yl)methanol (250. g, 1.30 mol) in chloroform (2,500 ml). This was followed by the dropwise addition of a solution of thionyl chloride (232. g, 1.95 mol) in chloroform (500 ml), while maintaining the internal temperature at room temperature (60 minute addition time). The resulting solution was heated to reflux for 2 hours. After cooling to ambient temperature, the mixture was concentrated, and the resulting residue was dissolved in 3,000 ml of ethyl acetate. Adjustment of the pH to 7 was accomplished by the addition of triethylamine. The resulting mixture was filtered and the filtrate was concentrated and the residue was purified by flash column chromatography (ethylacetate/petroleum ether gradient) to afford 1-benzyl-2-(chloromethyl)pyrrolidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08455477B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-d21cc5e537544f998cf5b95260a136fc |
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| Source note | uspto-grants-2013_06 |
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