HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080913Generated: October 28, 2026
Thionyl Chloride → 3-Ethynylbenzoyl chloride
https://huagongshe.com/reaction/2080913
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 a solution having 2.44 g (14.4 mmol) of diphenylamine dissolved in 7 ml of dichloromethane under ice-cooling and then the resultant mixture was stirred at room temperature for one hour. After completion of the stirring, dichloromethane 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/AcOEt10/1) using silica gel to obtain 0.7 g of 3-ethynyl-N,N-diphenylbenzamide which is a desired product as pale yellow liquid. (Yield: 35%)
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-3a81ddf554fc435b9301037574a49511 |
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| Source note | uspto-grants-2011_04 |
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