- 3-Bromo-1-indanone
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- $1.00 / 1KG
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2020-01-09
- CAS:40774-41-2
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: 200kg
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| | 3-Bromo-1-indanone Basic information |
| Product Name: | 3-Bromo-1-indanone | | Synonyms: | 3-Bromo-1-indanone;3-Bromoindan-1-one;1H-Inden-1-one, 3-broMo-2,3-dihydro-;3-Bromo-2,3-dihydro-1H-inden-1-one, 3-Bromo-2,3-dihydro-1-oxo-1H-indene;3-bromo-2,3-dihydroinden-1-one;3-Bromoindan-1-one 98%;3-Bromo-2,3-dihydro-1H-inden-1-one | | CAS: | 40774-41-2 | | MF: | C9H7BrO | | MW: | 211.06 | | EINECS: | | | Product Categories: | Fused Ring Systems;Halides | | Mol File: | 40774-41-2.mol |  |
| | 3-Bromo-1-indanone Chemical Properties |
| Melting point | 54.5-55 °C(Solv: carbon tetrachloride (56-23-5)) | | Boiling point | 271.3±39.0 °C(Predicted) | | density | 1.631±0.06 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | Appearance | Light yellow to yellow Solid |
| | 3-Bromo-1-indanone Usage And Synthesis |
| Synthesis | General procedure for the synthesis of 3-bromo-1-indanone from 1-indanone: 264 g (2.2 mol) of 1-indanone was dissolved in 154 mL of carbon tetrachloride, and 390 g (2.2 mol) of N-bromosuccinimide (non-caking powder) and 0.5 g of benzoyl peroxide were added. The reaction was refluxed under mechanical stirring for 1.5 hours. During the reaction, the color of the mixture changed abruptly to yellow and all N-bromosuccinimides (density greater than carbon tetrachloride) were converted to succinimides (density less than carbon tetrachloride). After completion of the reaction, the mixture was cooled to 20 °C, filtered and concentrated in vacuum. The crude product, 3-bromo-1-indanone, was dissolved in 600 mL of ethyl acetate/heptane (1:2) solvent mixture, cooled in an ice bath for 2 h, and subsequently crystallized in a refrigerator overnight to give 257 g of 3-bromo-1-indanone crystals in 62% yield. | | References | [1] Tetrahedron, 1995, vol. 51, # 32, p. 8953 - 8958
[2] Indian journal of chemistry, 1981, vol. 20 B, # 4, p. 303 - 307
[3] Patent: US2008/58329, 2008, A1. Location in patent: Page/Page column 13
[4] Tetrahedron Letters, 2006, vol. 47, # 7, p. 1097 - 1099
[5] Tetrahedron, 2009, vol. 65, # 22, p. 4429 - 4439 |
| | 3-Bromo-1-indanone Preparation Products And Raw materials |
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