HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 497288Generated: October 29, 2026
Thioanisole → 2-(4-Bromophenyl)-1-[4-(methylthio)phenyl]ethanone
https://huagongshe.com/reaction/497288
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thioanisole | HCID 7520 | — |
| Reactant | Benzeneacetic acid, 4-bromo- | HCID 74654 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | 2-(4-Bromophenyl)-1-[4-(methylthio)phenyl]ethanone | HCID 11450067 | 52.3% |
Reaction Steps
4-Bromophenylacetic acid (10.8 g, 0.050 mol) was disolved in thionyl chloride (50 mL) and stirred for 30 min at 90° C. The mixture was concentrated and the residual oil was disolved in carbon disulfide (100 mL) and thioanisole (12.5 g, 0.10 mol) was added and the mixture was cooled to 0° C. and AlCl3 (14.7 g, 0.11 mol) was added portionwise. The mixture was stirred at room temperature for 16 h. The resultant dark green suspension was poured into ice water (150 mL) and extracted with CH2Cl2 (150 mL×2), washed with aqueous saturated NaHCO3 (50 mL), dried over MgSO4, and concentrated in vacuo gave the solid. The solid was suspended in ether and collected by filtration to give the title compound (8.4 g, 46%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06949536B2 |
|---|
| Source dataset | uspto-grants-2005_09 |
|---|
| ORD ID | ord-27033eb6f8eb4fa49fd9598ab91f58ea |
|---|
| Source note | uspto-grants-2005_09 |
|---|