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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581700Generated: October 31, 2026

Ethanol → HCID 67596793, compound

https://huagongshe.com/reaction/581700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant2-Amino-2,3-dihydro-1H-inden-1-oneHCID 414531—
ReactantSodiumHCID 5360545—
ReactantHCID 86754188HCID 86754188—
SolventTolueneHCID 1140—
ProductHCID 67596793HCID 67596793—

Reaction Steps

2-Amino-6-chloro-1-indanone hydrochloride is prepared in the same way as in Example 1 for the preparation of 2-amino-1-indanone, starting from 57.5 g of 6-chloro-1-indanone oxime p-toluenesulphonate, 3.94 g of sodium, 200 ml of absolute ethanol and 1 litre of anhydrous toluene. After 15 hours of reaction at 0° C., the precipitate formed is filtered off on Celite, the filtrate washed with water and then extracted with IN hydrochloric acid (2×500 ml) and the aqueous phase concentrated to dryness under reduced pressure. 10.5 g of expected product are obtained in the form of a brown-green solid, the melting point of which is above 260° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922716
Source datasetuspto-grants-1999_07
ORD IDord-24925a6c0e5649589f0df39f7b2822c1
Source noteuspto-grants-1999_07