1-(4-BROMOPHENYL)CYCLOPROPANECARBOXYLIC ACID
1-(4-BROMOPHENYL)CYCLOPROPANECARBOXYLIC ACID Basic information
- Product Name:
- 1-(4-BROMOPHENYL)CYCLOPROPANECARBOXYLIC ACID
- Synonyms:
-
- 1-(4-BROMOPHENYL)CYCLOPROPANECARBOXYLIC ACID
- 1-(4-BroMophenyl)-1-cyclopropanecarboxylic acid
- Cyclopropanecarboxylic acid, 1-(4-broMophenyl)-
- 1-(4-broMophenyl)cyclopropane-1-carboxylic acid
- EOS-60374
- 345965-52-8, MFCD07374439
- CAS:345965-52-8
- CAS:
- 345965-52-8
- MF:
- C10H9BrO2
- MW:
- 241.08
- Product Categories:
-
- pharmacetical
- Carboxylic Acids
- Carboxylic Acids
- Ring Systems
- Mol File:
- 345965-52-8.mol
1-(4-BROMOPHENYL)CYCLOPROPANECARBOXYLIC ACID Chemical Properties
- Melting point:
- 160-165°
- Boiling point:
- 354.3±35.0 °C(Predicted)
- Density
- 1.670±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- form
- solid
- pka
- 4.14±0.20(Predicted)
- Appearance
- White to light yellow Solid
- InChI
- InChI=1S/C10H9BrO2/c11-8-3-1-7(2-4-8)10(5-6-10)9(12)13/h1-4H,5-6H2,(H,12,13)
- InChIKey
- BYJIXWOWTNEVFO-UHFFFAOYSA-N
- SMILES
- C1(C2=CC=C(Br)C=C2)(C(O)=O)CC1
1-(4-BROMOPHENYL)CYCLOPROPANECARBOXYLIC ACID Usage And Synthesis
Synthesis
124276-67-1
345965-52-8
General procedure for the synthesis of 1-(4-bromophenyl)cyclopropanecarboxylic acid from 1-(4-bromophenyl)cyclopropanecarbonitrile: A mixture of 1-(4-bromophenyl)cyclopropanecarbonitrile (7.5 g, 33.78 mmol), potassium hydroxide (7.6 g, 135 mmol), and ethylene glycol (50 mL) was heated to 160 °C for 6 hours. Upon completion of the reaction, the mixture was cooled to room temperature, water (200 mL) was added and the pH was adjusted to 3~4 with dilute hydrochloric acid to acidify the reaction mixture. Subsequently, the product was precipitated with 2N hydrochloric acid. The precipitate was collected by filtration to afford 1-(4-bromophenyl)cyclopropanecarboxylic acid (5.6 g, 69% yield). Mass spectrum (ESI) m/z (M+H)+ 240.
References
[1] Patent: US6359135, 2002, B1. Location in patent: Page column 113
[2] Patent: US6369225, 2002, B1. Location in patent: Page column 42, 112
[3] Journal of Medicinal Chemistry, 2010, vol. 53, # 16, p. 6003 - 6017
[4] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 3, p. 887 - 892
[5] Patent: WO2013/25733, 2013, A1. Location in patent: Paragraph 0490
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