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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461880Generated: October 26, 2026

Ammonium Acetate → 2-(Aminomethylidene)-2,3-dihydro-1h-inden-1-one

https://huagongshe.com/reaction/461880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
Reactant2-Hydroxy-methylene-1-indanoneHCID 70601221—
SolventEthanolHCID 702—
Product2-(Aminomethylidene)-2,3-dihydro-1h-inden-1-oneHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04064272
Source datasetuspto-grants-1977_12
ORD IDord-c0e3065d575b45bd855dd63e2ea02164
Source noteuspto-grants-1977_12