HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 442924Generated: October 31, 2026
3-Methylbenzenesulphonyl chloride → HCID 10934765, compound
https://huagongshe.com/reaction/442924
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Methylbenzenesulphonyl chloride | HCID 2734595 | — |
| Reactant | Resorcinol, 5-methyl-, monohydrate | HCID 3083941 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 10934765 | HCID 10934765 | 94.3% |
Reaction Steps
Orcinol monohydrate (1.42 g, 10.0 mmol) and 3-methylbenzenesulfonyl chloride (1.60 g, 8.0 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 (3×40 mL). The organic phase was washed with brine (2×30 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 yellow oil (2.1 g, 76%). 1H-NMR (300 MHz, CDCl3) δ 7.68 (s, 1H), 7.64 (d, J=7.9 Hz, 1H), 7.45 (t, J=7.8 Hz, 1H), 7.40 (t, J=7.6 Hz, 1H), 6.54 (s, 1H), 6.39 (s, 1H), 6.32 (s, 1H), 5.33 (s, 1H), 2.41 (s, 3H), 2.21 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05891909 |
|---|
| Source dataset | uspto-grants-1999_04 |
|---|
| ORD ID | ord-71004d10adc34bdd82d652e390f27bb6 |
|---|
| Source note | uspto-grants-1999_04 |
|---|