HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981246Generated: October 30, 2026
2-Naphthalenesulfonyl chloride → HCID 14424883, compound
https://huagongshe.com/reaction/981246
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Naphthalenesulfonyl chloride | HCID 7125 | — |
| Reactant | 2-Pyrrolidone | HCID 12025 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 14424883 | HCID 14424883 | 58% |
Reaction Steps
15.6 cm3 of a 1.6M solution of butyllithium in hexane is added to 2.13 g of 2-pyrrolidinone in solution in 80 cm3 of tetrahydrofuran, cooled to -10° C., maintaining the temperature between -5° C. and +5° C. After agitation at -5° C. for 25 minutes, 6.12 g of beta-naphthalene-sulphonyl chloride is added, without exceeding 0° C. The whole is then left to return to ambient temperature. The solvent is evaporated off under reduced pressure, the residue is taken up in ethyl acetate, and the lithium chloride is filtered off and after evaporating under reduced pressure, the residue is taken up in water and filtered. Finally after crystallization from isopropanol, 4 g of expected product is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04990531 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-16e2b550c3904cc582d90bc6e9b247bb |
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| Source note | uspto-grants-1991_02 |
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