The invention relates to a new synthesis method of 5-aminoindanone (compound III), and mainly solves the technical problems of long reaction route, a lot of waste acid and difficult after-treatment, not readily available raw materials and the like in existing synthesis methods. The method provided by the invention includes: reacting aniline (compound I) with 3-chloropropionylchloride to obtain a compound II, and subjecting II to microwave reaction to obtain the compound III.

Synthesis method of 5-aminoindanone

Indeno-furan ketones compound with bioactivities and method for preparing same

The invention discloses an indeno oxa-carboxylic acid derivative with insecticidal, acaricidal and/or bactericidal bioactivities in a formula (I), a method for preparing same and an application thereof, wherein R is C1-C3 alkyl; R1 is H or halogen; and R2 is halogen and phenyl, and the phenyl is substituted by at most 5 same or different substituent groups which are selected from the following list: H, halogen, C1-C3 alkyl, C1-C3 halogenated alkyls, C1-C3 alkoxy and C1-C3 halogenated alkoxy. The indeno oxa-carboxylic acid derivative has bioactivities, and has the acaricidal, insecticidal and bactericidal bioactivities under the usage of 2.5-5000mg/L.

Indeno oxa-carboxylic acid derivative with bioactivities and method for preparing same

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Indeno-furan ketones compound with bioactivities and method for preparing same

Indeno oxa-carboxylic acid derivative with bioactivities and method for preparing same