HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080922Generated: October 30, 2026
3-Ethynylbenzoyl chloride → HCID 86634500, compound
https://huagongshe.com/reaction/2080922
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Ethynylbenzoyl chloride | HCID 20038813 | — |
| Reactant | Sodium benzenethiol | HCID 66586497 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86634500 | HCID 86634500 | — |
Reaction Steps
Air in a 20 ml Schlenk tube was replaced by Ar gas and 1.02 g (7 mmol) of m-ethynylbenzoic acid and 5 g (42 mmol) of thionyl chloride were added to the tube and the mixture was stirred at 50° C. for 2 hours and then excess thionyl chloride was removed by distillation under reduced pressure to obtain m-ethynylbenzoyl chloride. To the m-ethynylbenzoyl chloride obtained was added 7 ml of THF and the resultant mixture was ice-cooled. Then, 971 mg (7.35 mmol) of sodium benzenethiol was added to the mixture and the resultant mixture was stirred at room temperature for 2 hours. After completion of the stirring, THF was removed by distillation under reduced pressure and 35 ml of water was added to the resultant residue. The mixture was extracted with 35 ml of ethyl acetate, the extract was dried over magnesium sulfate and the solvent was removed by distillation under reduced pressure using an evaporator. The resultant crude reaction product was purified by column chromatography (Hexane/AcOEt=20/1) using silica gel to obtain 0.51 g of S-phenyl 3-ethynyl-thiobenzoate which is a desired product as yellow solid. (Yield: 31%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932398B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-862c73b5cecd4d6eb640c817fff56de3 |
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| Source note | uspto-grants-2011_04 |
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