HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1980840Generated: November 1, 2026
Water → N-(1,1-dimethyl-4-indanyl)-o-methylbenzamide
https://huagongshe.com/reaction/1980840
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Methylbenzoyl chloride | HCID 70276 | — |
| Reactant | 1,1-Dimethyl-2,3-dihydro-1H-inden-4-amine | HCID 13115615 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(1,1-dimethyl-4-indanyl)-o-methylbenzamide | HCID 13268043 | 93.9% |
Reaction Steps
A solution of 0.81 g of o-methylbenzoyl chloride (5.25 m mol) in 3 ml of tetrahydrofuran is added dropwise to a solution of 0.81 g of 1,1-dimethyl-4-aminoindan (5.00 m mol) and 0.61 g of triethylamine (6.00 m mol) in 10 ml of tetrahydrofuran, while maintaining the reaction mixture at 0° C. by ice-cooling. Then, reaction mixture is stirred over night at room temperature, and water and ethyl acetate are added to the mixture. The organic layer is washed with 5% hydrochloric acid and water and dried over anhydrous sodium sulfate. After the solvent is removed by distillation, the residue is dried to give 1.31 g of N-(1,1-dimethyl-4-indanyl)-o-methylbenzamide (yield: 93.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04511581 |
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| Source dataset | uspto-grants-1985_04 |
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| ORD ID | ord-f3a9a146354041b1b3b03d921da5ed0a |
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| Source note | uspto-grants-1985_04 |
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