HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1438936Generated: October 26, 2026
Hydrochloric Acid → 6-Benzoyl-indane-1-carboxylic acid methyl ester
https://huagongshe.com/reaction/1438936
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Methyl 2,3-dihydro-1H-indene-1-carboxylate | HCID 3839612 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Product | 6-Benzoyl-indane-1-carboxylic acid methyl ester | HCID 53662138 | — |
Reaction Steps
18 g of finely powdered aluminum chloride are added in portions of a solution of 8 g of indane-1-carboxylic acid methyl ester and 8.2 g of benzoyl chloride in 100 ml of carbon disulphide, whilst stirring in an anhydrous atmosphere. After completion of the addition, the reaction mixture is heated for 2 hours to the reflux temperature. It is then allowed to cool to room temperature, poured onto a mixture of 100 g of ice and 50 ml of concentrated hydrochloric acid and extracted with twice 100 ml of ether. The organic phases are combined, washed with twice 100 ml of water, dried over sodium sulphate and evaporated in vacuo. Distillation of the evaporation residue in a high vacuum gives 6-benzoyl-indane-1-carboxylic acid methyl ester in the fraction boiling at 165°-170° C (0.5 mm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04057573 |
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| Source dataset | uspto-grants-1977_11 |
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| ORD ID | ord-c9e7fc09d4244291a0b2ccfc21e4ac16 |
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| Source note | uspto-grants-1977_11 |
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