HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357674Generated: October 30, 2026
Hydrochloric Acid → HCID 22172983, compound
https://huagongshe.com/reaction/357674
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 18938318 | HCID 18938318 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22172983 | HCID 22172983 | — |
Reaction Steps
A solution of 193 g (0.80 mol) of 2-(2-(2-(pyridyl)benzyl)propionic acid in 81 cm3 (1.2 mol) of thionyl chloride was stirred at room temperature for 18 hours. Excess thionyl chloride was removed at 10 mbar and the acid chloride was taken up in 400 cm3 of toluene. The solution was added dropwise at 10° C. to a suspension of 113 g (0.85 mol) of AlCl3 in 1500 cm3 of toluene and heated at 80° C. for 1 hour. The reaction mixture was poured onto 2000 g of ice and acidified with concentrated aqueous HCl to a pH of 1. The organic phase was separated off and the aqueous phase was further extracted 3 times with 200 cm3 each time of Et2O. The combined organic phases were washed with saturated aqueous NaHCO3 solution and saturated aqueous NaCl solution and subsequently dried (MgSO4). This gave 132 g (74%) of 2-methyl-4-(2-pyridyl)-1-indanone which was further reacted without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05840947 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-5657f2fe9dbe4b26aff8b9b325e8e7ca |
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| Source note | uspto-grants-1998_11 |
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