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200049-46-3

7-bromoisoindolin-1-one

CAS: 200049-46-3

Molecular Formula: C8H6BrNO

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200049-46-3 - Names and Identifiers

Name 7-bromoisoindolin-1-one
Synonyms 7-Bromoisoindolinone
7-Bromo-1-isoindolinone
7-bromoisoindolin-1-one
7-Bromo-2,3-dihydro-isoindol-1-one
7-bromo-2,3-dihydro-isoindole-1-one
7-bromo-2,3-dihydro-1H-isoindol-1-one
7-broMo-2,3-dihydro-1H-isoindol-1-one
1H-Isoindol-1-one, 7-broMo-2,3-dihydro-
1H-Isoindol-1-one, 7-bromo-2,3-dihydro-
CAS 200049-46-3
InChI InChI=1/C8H6BrNO/c9-6-3-1-2-5-4-10-8(11)7(5)6/h1-3H,4H2,(H,10,11)

200049-46-3 - Physico-chemical Properties

Molecular FormulaC8H6BrNO
Molar Mass212.04
Density1.666±0.06 g/cm3(Predicted)
Boling Point452.2±45.0 °C(Predicted)
Flash Point227.266°C
Vapor Presure0mmHg at 25°C
pKa13.36±0.20(Predicted)
Storage ConditionSealed in dry,Room Temperature
Refractive Index1.625

200049-46-3 - Reference Information

Uses 7-bromo-2, 3-dihydro-isoindole-1-one is a useful research chemical for organic synthesis and other chemical processes.
Preparation The condensation reaction of o-halomethyl or o-acyl benzoate with amines is a traditional method for synthesizing iso-indole ketone compounds. The selective reduction of phthalimide and various organic transformations of benzo [c] pyrrolidone derivatives are also used to synthesize iso-indole ketone derivatives. In this paper, the target compound 7-bromo-2, 3-dihydro-isoindole-1-one was prepared by ring-closing reaction with methyl 2-bromomethyl-3-chlorobenzoate and liquid ammonia as starting materials. The synthesis reaction formula is as follows: Experimental operation: Methyl 2-bromomethyl-3-chlorobenzoate and liquid ammonia are reacted in 20 mL methanol solution at 60°C under stirring to the end point (TLC detection). Chilled to room temperature, extracted with ethyl acetate, the organic phase was washed with saturated salt water for 3 times, anhydrous sodium sulfate was dried, concentrated and evaporated, and the residue was purified by silica gel column chromatography (eluent: ethyl acetate/petroleum ether, V/ V = 1/5) to obtain compound 7-bromo-2, 3-dihydro-indole-1-one.
Last Update:2024-04-09 02:00:01
200049-46-3
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