HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713305Generated: November 3, 2026
Water → 4-(3-Hydroxypropylsulfanyl)phenylbenzonitrile
https://huagongshe.com/reaction/1713305
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Cyanophenylboronic acid | HCID 2734326 | — |
| Reactant | 3-(3-Bromophenylsulfanyl)propane-1-ol | HCID 58522097 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(3-Hydroxypropylsulfanyl)phenylbenzonitrile | HCID 67454812 | 71.2% |
Reaction Steps
3-(3-Bromophenylsulfanyl)propane-1-ol (0.49 g) was suspended in acetonitrile (8.5 mL), 4-cyanophenylboronic acid (0.34 g), sodium carbonate (0.42 g), water (1.7 mL) and tetrakis(triphenylphosphine)palladium(0) (0.12 g) were added, and the resulting mixture was stirred at 80° C. for 7 hours. The reaction mixture was cooled to room temperature and then partitioned between ethyl acetate (35 mL) and water (10 mL). The organic layer was washed successively with water (10 mL) and brine (10 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: hexane/ethyl acetate=2/1) to give the title compound (0.38 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07795236B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-ad5c31d107e24ae6804bfbd2b1c92f9e |
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| Source note | uspto-grants-2010_09 |
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