Identification | More | [Name]
4-CHLORO-3-METHOXYBENZOIC ACID | [CAS]
85740-98-3 | [Synonyms]
4-CHLORO-3-METHOXYBENZOIC ACID TIMTEC-BB SBB008504 4-CHLORO-3-METHOXYBENZOIC ACID---POWDER--- | [Molecular Formula]
C8H7ClO3 | [MDL Number]
MFCD00269640 | [Molecular Weight]
186.59 | [MOL File]
85740-98-3.mol |
Safety Data | Back Directory | [Hazard Codes ]
T,N | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [RIDADR ]
3077 | [WGK Germany ]
3 | [HazardClass ]
9 | [PackingGroup ]
Ⅲ | [HS Code ]
2918999090 |
Hazard Information | Back Directory | [Uses]
4-Chloro-3-methoxybenzoic acid can be used to synthesize specific drug molecules, such as a key intermediate for the antiarrhythmic drug amiodarone. | [Synthesis]
B. Synthesis of 4-chloro-3-methoxybenzoic acid (0200)
To crude 1-chloro-2-methoxy-4-methylbenzene (7.8 g, 50 mmol) was added an aqueous solution of potassium permanganate (KMnO4, 19.8 g, 125 mmol) (300 mL). The reaction mixture was stirred vigorously under reflux conditions for 17 h. After completion of the reaction, the filter was passed through diatomaceous earth and the filter cake was washed with hot water (200 mL). The clarified filtrate was washed with ether (2 x 150 mL) and then acidified with concentrated hydrochloric acid (HCl) to pH < 2. After addition of concentrated hydrochloric acid (9 mL), the precipitate was collected by filtration to give pure white solid 4-chloro-3-methoxybenzoic acid (5.36 g, 58% yield). Electrospray mass spectrometry (ES-MS) showed (M + H)+ peak located at m/z = 187. | [References]
[1] Journal of Medicinal Chemistry, 1992, vol. 35, # 23, p. 4408 - 4414 [2] European Journal of Medicinal Chemistry, 2011, vol. 46, # 12, p. 5754 - 5762 [3] Archiv der Pharmazie, 2011, vol. 344, # 11, p. 745 - 754 [4] Chemical Biology and Drug Design, 2013, vol. 82, # 3, p. 336 - 347 [5] European Journal of Medicinal Chemistry, 2013, vol. 65, p. 315 - 322 |
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