HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476645Generated: October 30, 2026
Benzenesulfonyl chloride → HCID 21611515, compound
https://huagongshe.com/reaction/476645
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | HCID 19838059 | HCID 19838059 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 21611515 | HCID 21611515 | 31.9% |
Reaction Steps
39.37 cm3 of a 1.4M solution of n-butyllithium in n-hexane is added to a solution of 10.1 g of 1,5-dihydro-5-n-hexyloxy-2H-pyrrol-2-one obtained at stage A in 170 cm3 of tetrahydrofuran cooled to -30° C. The temperature is maintained at -30° C. while agitating for 15 minutes, then is reduced to -35° C. and a solution of 9.73 g of benzenesulphonyl chloride in 70 cm3 of tetrahydrofuran is added, while maintaining the temperature at between -35° C. and -53° C. The temperature is allowed to return to the ambient, the solvent is evaporated under reduced pressure, and the residue is chromatographed on silica (eluent: ethyl acetate-n-hexane, 1-2). 5.68 g of the expected product is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04885307 |
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| Source dataset | uspto-grants-1989_12 |
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| ORD ID | ord-942ee61af7f54735aa13df1bf9286ced |
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| Source note | uspto-grants-1989_12 |
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