HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436179Generated: October 31, 2026
Acetone → 6-Benzoyl-2,3-dihydro-1H-indene-1-carboxamide
https://huagongshe.com/reaction/436179
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Dichromate | HCID 25408 | — |
| Reactant | HCID 20310092 | HCID 20310092 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Benzoyl-2,3-dihydro-1H-indene-1-carboxamide | HCID 12318512 | — |
Reaction Steps
To 150 ml. of acetone is added 12.5 g. of 6-benzylindan-1-carboxamide, followed by the dropwise addition of a solution of 5 g. of sodium dichromate in 24 ml. of 6N sulfuric acid. After the addition has been completed, the mixture is stirred overnight. Then 200 ml. of water is added and the acetone is distilled off under reduced pressure. The residue is extracted with ethyl acetate. The extract is washed with water and dried, followed by removal of the solvent by distillation under reduced pressure. The residue is purified by column chromatography (500 g. of silica gel; eluted with a 7:3 solvent mixture of chloroform and acetone) and the resultant crude crystals are recrystallized from benzene. The procedure gives 6-benzoylindan-1-carboxamide as crystals melting at 195°-197° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04007225 |
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| Source dataset | uspto-grants-1977_02 |
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| ORD ID | ord-fe13e02733f34bd6951e58e0d0573772 |
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| Source note | uspto-grants-1977_02 |
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