HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108638Generated: October 30, 2026
Ethyl Acetate → 3,5-Dimethyl-4-(3'-iso-propyl-4'-methoxyphenylsulfanyl)anisole
https://huagongshe.com/reaction/2108638
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Iodo-5-methoxy-1,3-dimethylbenzene | HCID 14720601 | — |
| Reactant | 4-Methoxy-3-iso-propyl-thiophenol | HCID 22726990 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | HCID 178505378 | HCID 178505378 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3,5-Dimethyl-4-(3'-iso-propyl-4'-methoxyphenylsulfanyl)anisole | HCID 66642821 | 49% |
Reaction Steps
Copper iodine (70 mg, 0.37 mmol), neocuprinine (80 mg, 0.37 mmol) and potassium t-butoxide (470 mg, 4.05 mmol) were added in this order to a solution of 4-methoxy-3-iso-propyl-thiophenol (U.S. Pat. No. 6,747,048 B2, 600 mg, 2.3 mmol) and 3,5-dimethyl-4-iodoanisole (678 mg, 3.72 mmol) in toluene (10 mL). After refluxing overnight, the cooled reaction mixture was poured into ethyl acetate (50 mL) and washed twice with 1 N HCl then brine. The organics were dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel, hexane/ethyl acetate 100:0 to 40:1) to give 3,5-dimethyl-4-(3′-iso-propyl-4′-methoxyphenylsulfanyl)anisole (0.358 g, 49%); 1H NMR (200 MHz, DMSO-d6): δ 6.87-6.80(m, 4H), 6.56(m, 1H), 3.76(s, 3H), 3.71(s, 3H), 3.15(m, 1H), 2.34(s, 6H), 1.06(d, 6H, J=7 Hz); TLC conditions: Uniplate silica gel, 250 microns; Mobile phase=25% ethyl acetate in hexane; Rf=0.36
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07514419B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-532d5fe85fa748738e4cae33833d6c1b |
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| Source note | uspto-grants-2009_04 |
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