HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1993040Generated: October 30, 2026
Hydrochloric Acid → 4-(2-Methyl-benzylsulfanyl)-benzaldehyde
https://huagongshe.com/reaction/1993040
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Reactant | (2-Methylphenyl)methanethiol | HCID 288028 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(2-Methyl-benzylsulfanyl)-benzaldehyde | HCID 59132706 | 57.1% |
Reaction Steps
4-fluoro-benzaldehyde (1.16 g, 9.32 mmol) was added dropwise over 2 minutes to a solution of o-tolyl-methanethiol (1.35 g, 9.79 mmol) and Cesium carbonate (3.19 g, 9.79 mmol) in DMF (20 mL). The solution was stirred at 40° C. overnight and then poured into copious water. The pH of the solution was adjusted to 4 with 1N HCl(aq), and the aqueous solution was extracted with ethyl acetate (2×35 mL). The combined organic layers were washed with water, followed by brine. The combined organic layers were then dried (Na2SO4) and the solvent removed under reduced pressure. The resulting residue was purified via radial chromatography (15% ethyl acetate in hexanes) to yield 1.29 g (54%) of 4-(2-Methyl-benzylsulfanyl)-benzaldehyde (28.1). LC/MSD mle: 243.0 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07649110B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-8a96f6e669a747c08d61211eaf23cdb0 |
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| Source note | uspto-grants-2010_01 |
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