HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442976Generated: October 29, 2026
3-Cyanobenzene-1-sulfonyl chloride → HCID 54212462, compound
https://huagongshe.com/reaction/442976
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Cyanobenzene-1-sulfonyl chloride | HCID 2801360 | — |
| Reactant | Resorcinol, 5-methyl-, monohydrate | HCID 3083941 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 54212462 | HCID 54212462 | 83% |
Reaction Steps
Orcinol monohydrate (1.42 g, 10.0 mmol) and 3-cyanobenzenesulfonyl chloride (2.02 g, 10.0 mmol) were mixed in saturated aqueous NaHCO3 (30 mL) and diethyl ether (30 mL). The biphasic mixture was stirred vigorously at ambient temperature overnight. The reaction mixture was diluted with water (50 mL) and extracted into ethyl acetate (3×50 mL). The organic phase was washed with brine (2×50 mL) and dried over Na2SO4. After removing the solvent in vacuo, the residue was purified by flash column chromatography (dichloromethane to 5% ethyl acetate in dichloromethane) to give the title compound as a pale yellow oil (2.40 g, 83%). 1H-NMR (300 MHz, CDCl3) δ 8.12 (s, 1H), 8.07 (d, J=8.0 Hz, 1H), 7.93 (d, J=7.8 Hz, 1H), 7.68 (t, J=7.9 Hz, 1H), 6.56 (s, 1H), 6.36 (s, 1H), 6.30 (s, 1H), 5.35 (s, 1H), 2.22 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05891909 |
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| Source dataset | uspto-grants-1999_04 |
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| ORD ID | ord-d3e2707b77eb4087807400f39ec42584 |
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| Source note | uspto-grants-1999_04 |
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