HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461880Generated: October 27, 2026
Ammonium Acetate → 2-(Aminomethylidene)-2,3-dihydro-1h-inden-1-one
https://huagongshe.com/reaction/461880
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 2-Hydroxy-methylene-1-indanone | HCID 70601221 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(Aminomethylidene)-2,3-dihydro-1h-inden-1-one | HCID 170312 | — |
Reaction Steps
To a stirred solution of 2-hydroxy-methylene-1-indanone (1.6 kg. as a 3.7 kg. wet cake) dissolved in ethanol (30 liters), and under a nitrogen atmosphere was added ammonium acetate (1.92 kg. 24.8 mole). After eight hours the reaction was complete and the ethanol was removed by vacuum distillation. The reaction mixture was cooled to room temperature and after filtration and air drying (1 hr.) yielded crude 2-aminomethylene-1-indanone (I) as orange crystals. The crystals were then dissolved in a minimum amount of hot ethanol and the solution was decolorized with activated charcoal. Crystals appeared in the filtrate and after cooling overnight at 5° C, the reaction mixture was filtered yielding 960 gm. of compound (I) as light orange crystals. The filtrate was again treated with activated charcoal and recrystallized providing an additional 200 gm. of compound (I). The combined sample (1160 gm.) was milled giving a fine yellowish powder which was dried at 50° C/25 mm/Hg for 48 hours. A sample (50 gm.) of this material was recrystallized three times from ethanol to give 2-aminomethylene-1-indanone (15 gm.), m.p. 166°-168° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04064272 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-c0e3065d575b45bd855dd63e2ea02164 |
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| Source note | uspto-grants-1977_12 |
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