7-chloro-4-oxo-4H-chromene-2-carboxylic acid
7-chloro-4-oxo-4H-chromene-2-carboxylic acid Basic information
- Product Name:
- 7-chloro-4-oxo-4H-chromene-2-carboxylic acid
- Synonyms:
-
- 7-chloro-4-oxo-4H-chromene-2-carboxylic acid
- 4H-1-Benzopyran-2-carboxylic acid, 7-chloro-4-oxo-
- CAS:
- 114741-22-9
- MF:
- C10H5ClO4
- MW:
- 224.6
- Mol File:
- 114741-22-9.mol
7-chloro-4-oxo-4H-chromene-2-carboxylic acid Chemical Properties
- Melting point:
- >244oC (dec.)
- storage temp.
- Sealed in dry,Room Temperature
- solubility
- DMSO (Slightly), Methanol (Slightly)
- form
- Solid
- color
- PaleYellow to Pale Beige
7-chloro-4-oxo-4H-chromene-2-carboxylic acid Usage And Synthesis
Synthesis
113850-94-5
114741-22-9
The general procedure for the synthesis of 7-chloro-4-oxo-4H-chromene-2-carboxylic acid from ethyl 7-chloro-4-oxo-4H-chromene-2-carboxylate was as follows: an aqueous 6M HCl solution (2 mL) was added to a solution of ethyl 7-chloro-4-oxo-4H-chromene-2-carboxylate in acetic acid (4 mL) and the mixture was heated to 80 °C and kept for 4.5 hours. After completion of the reaction, the mixture was cooled to room temperature, diluted with distilled water (6 mL), the resulting beige precipitate (204 mg, 89% yield) was collected by filtration and dried under reduced pressure at 50 °C. The product was characterized by 1H NMR (300 MHz, DMSO-d6): δ 6.92 (s, 1H), 7.58 (dd, J = 8.65,1.86 Hz, 1H), 7.95 (d, J = 1.70 Hz, 1H), 8.04 (d, J = 8.48 Hz, 1H); mass spectrum (APCI) m/z 225 [M + H]+, 224 [ M-H]+, 178.9 [M-CO2H]+.
References
[1] Patent: US2005/209274, 2005, A1. Location in patent: Page/Page column 22
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