HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080921Generated: October 28, 2026
Thionyl Chloride → 3-Ethynylbenzoyl chloride
https://huagongshe.com/reaction/2080921
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-Ethynylbenzoic acid | HCID 15897047 | — |
| Product | 3-Ethynylbenzoyl chloride | HCID 20038813 | — |
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-165b685ea5744663a88f4d26cfa90ab4 |
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| Source note | uspto-grants-2011_04 |
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