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Product Details of [ 302553-00-0 ]

CAS No. :302553-00-0
Formula : C10H6BrNO3
M.W : 268.06
SMILES Code : O=C(C1=CNC2=C(C=C(Br)C=C2)C1=O)O
MDL No. :MFCD01909532

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* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 302553-00-0 ]

[ 302553-00-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 122794-99-4 ]
  • [ 302553-00-0 ]
YieldReaction ConditionsOperation in experiment
99% With sodium hydroxide; In ethanol; water monomer; for 3h;Reflux; 77ml aqueous NaOH (2 N) were added at ambient temperature to asuspension of 15.2 g of the product from the previous step (51.2mmol) in 77 ml EtOH. The mixture was heated to reflux for 3 h andthen concentrated to approx. 50% of the starting volume. The yellowsolution was diluted with water and cooled with an ice bath.The mixture was acidified to pH 2 with hydrochloric acid to precipitatethe product. The resulting suspension was stirred for 10min at low temperature and was then filtered via a Buchner funnel.The filter cakewaswashed with H2O and dried in a convection ovenat 80 C to yield 13.5 g (99%) of the title compound as white solid. 1HNMR (200 MHz, DMSO) d 14.97 (br s, 1H), 13.56 (br s, 1H), 8.90 (s,1H), 8.30 (d, J 2.3 Hz, 1H), 8.00 (dd, J 8.9, 2.3 Hz, 1H), 7.75 (d, J 8.9 Hz, 1H) 13C NMR (50 MHz, DMSO) d 177.1, 166.0, 145.6, 138.4,136.6, 127.1, 125.9, 122.1, 119.0, 108.1. ESI-MS m/z: 265.6 [M H]-HPLC (Method A) tret 6.16 min.
99% With sodium hydroxide; In ethanol; water monomer; for 3h;Reflux; 77ml aqueous NaOH (2 N) were added at ambient temperature to asuspension of 15.2 g of the product from the previous step (51.2mmol) in 77 ml EtOH. The mixture was heated to reflux for 3 h andthen concentrated to approx. 50% of the starting volume. The yellowsolution was diluted with water and cooled with an ice bath.The mixture was acidified to pH 2 with hydrochloric acid to precipitatethe product. The resulting suspension was stirred for 10min at low temperature and was then filtered via a Buchner funnel.The filter cakewaswashed with H2O and dried in a convection ovenat 80 C to yield 13.5 g (99%) of the title compound as white solid. 1HNMR (200 MHz, DMSO) d 14.97 (br s, 1H), 13.56 (br s, 1H), 8.90 (s,1H), 8.30 (d, J 2.3 Hz, 1H), 8.00 (dd, J 8.9, 2.3 Hz, 1H), 7.75 (d, J 8.9 Hz, 1H) 13C NMR (50 MHz, DMSO) d 177.1, 166.0, 145.6, 138.4,136.6, 127.1, 125.9, 122.1, 119.0, 108.1. ESI-MS m/z: 265.6 [M H]-HPLC (Method A) tret 6.16 min.
96% With water monomer; sodium hydroxide; In ethanol; at 75℃; for 1.5h; 2N Sodium hydroxide (506mL, 1011.43mmol) was added to a stirred suspension of ethyl 6-bromo-4-oxo-lH-quinoline-3-carboxylate (59.9g, 202.29mmol) in EtOH (590mL) and the resulting solution stirred at 75C for 1.5 h. Water was added and the mixture cooled to 0C. The pH of the solution was adjusted to 3 using hydrochloric acid and the precipitate collected by filtration. The solid was washed with water, EtOH/water (1 : 1) then Et20 before being dried to afford the desired material (51.9g, 96%) as a beige solid. NMR Spectrum: 1H MR (500MHz, DMSO-d6) δ 7.80 (1H, d), 8.05 (1H, d), 8.37 (1H, s), 8.93 (1H, s). Mass Spectrum: m/z (ES+)[M+H]+ = 270.
 

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• Alkyl Halide Occurrence • Arndt-Eistert Homologation • Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Clemmensen Reduction • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Fischer Indole Synthesis • General Reactivity • Grignard Reaction • Henry Nitroaldol Reaction • Hiyama Cross-Coupling Reaction • Horner-Wadsworth-Emmons Reaction • Hunsdiecker-Borodin Reaction • Hydride Reductions • Kinetics of Alkyl Halides • Kumada Cross-Coupling Reaction • Lawesson's Reagent • Leuckart-Wallach Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Peterson Olefination • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Amines • Preparation of Carboxylic Acids • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Carboxylic Acids • Reactions of Dihalides • Reformatsky Reaction • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Ketenes • Stille Coupling • Stobbe Condensation • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • Tebbe Olefination • Ugi Reaction • Wittig Reaction • Wolff-Kishner Reduction

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