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[ CAS No. 140472-69-1 ] {[proInfo.proName]}

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Chemical Structure| 140472-69-1
Chemical Structure| 140472-69-1
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Product Details of [ 140472-69-1 ]

CAS No. :140472-69-1 MDL No. :MFCD06797980
Formula : C7H5BrO3 Boiling Point : -
Linear Structure Formula :- InChI Key :WGIBEMRBLBGETQ-UHFFFAOYSA-N
M.W : 217.02 Pubchem ID :15735511
Synonyms :

Safety of [ 140472-69-1 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P273-P301+P310-P305+P351+P338 UN#:2811
Hazard Statements:H301-H410 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 140472-69-1 ]

* 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 [ 140472-69-1 ]

[ 140472-69-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 42237-85-4 ]
  • [ 140472-69-1 ]
YieldReaction ConditionsOperation in experiment
66% With sulfuric acid; water; sodium nitrite; for 1.75h;Reflux; The title compound of Preparation 50 (5.80 g, 26.85 mmols), in 10% sulphuric acid (55 ml), was diazotised with sodium nitrite (1.85 g), and the solution boiled with dilute sulphuric acid (1:1) ( 30ml) for one hour and forty-five minutes. The solution was cooled at room temperature. The suspension was filtered and the solid give 3.83 g (66%) of the title compound. HPLC/MS (10 min) retention time 5.06 min LRMS: m/z 215 (M-1)
66% With sulfuric acid; water; sodium nitrite; In water; for 1.75h;Reflux; PREPARATION 22 3-Bromo-5-hydroxybenzoic acid The title compound of Preparation 21 (5.80 g, 26.85 mmols), in 10% sulphuric acid (55 mL), was diazotised with sodium nitrite (1.85 g), and the solution boiled with dilute sulphuric acid (1:1) (30 mL) for one hour and forty-five minutes. The solution was cooled at room temperature. The suspension was filtered and the solid give 3.83 g (66%) of the title compound. HPLC/MS (10 min) retention time 5.06 min LRMS: m/z 215 (M-1)
  • 2
  • [ 49851-36-7 ]
  • [ 140472-69-1 ]
  • methyl 2-(2-(3-bromo-5-hydroxybenzamido)phenyl)acetate [ No CAS ]
YieldReaction ConditionsOperation in experiment
TEA (2.248 mL, 16.13 mmol) was added to a mixture of 3-bromo-5-hydroxybenzoic acid (CAS 140472-69-1 ) (1000 mg, 4.61 mmol), <strong>[49851-36-7]methyl 2-(2-aminophenyl)acetate hydrochloride</strong> (CAS 49851-36-7) (978 mg, 4.61 mmol) and HATU (1927 mg, 5.07 mmol) in DMF (10 mL) at 23 C. The resulting mixture was stirred at rt overnight. To the mixture was added K2C03 (191 1 mg, 13.82 mmol) and the mixture was heated to 100 C for 2 hours. The reaction mixture was diluted with EtOAc and washed with water. The organic layer was concentrated and the residue was purified by flash column on silica gel (EtOAc-heptane 0-100%) to give the title compound. MS (ESI+) m/z 364.1 , 366.1 (M+1 ).
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Technical Information

? Acidity of Phenols ? Alkyl Halide Occurrence ? Appel Reaction ? Arndt-Eistert Homologation ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions ? Chan-Lam Coupling Reaction ? Chugaev Reaction ? Corey-Kim Oxidation ? Dess-Martin Oxidation ? Electrophilic Substitution of the Phenol Aromatic Ring ? Etherification Reaction of Phenolic Hydroxyl Group ? Friedel-Crafts Reaction ? General Reactivity ? Grignard Reaction ? Halogenation of Phenols ? Hiyama Cross-Coupling Reaction ? Hunsdiecker-Borodin Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Jones Oxidation ? Kinetics of Alkyl Halides ? Kumada Cross-Coupling Reaction ? Martin's Sulfurane Dehydrating Reagent ? Mitsunobu Reaction ? Moffatt Oxidation ? Oxidation of Alcohols by DMSO ? Oxidation of Phenols ? Passerini Reaction ? Pechmann Coumarin Synthesis ? Preparation of Alcohols ? Preparation of Aldehydes and Ketones ? Preparation of Alkylbenzene ? Preparation of Amines ? Preparation of Carboxylic Acids ? Reactions of Alcohols ? Reactions of Alkyl Halides with Reducing Metals ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reactions of Carboxylic Acids ? Reactions of Dihalides ? Reactions with Organometallic Reagents ? Reimer-Tiemann Reaction ? Ritter Reaction ? Schmidt Reaction ? Sharpless Olefin Synthesis ? Specialized Acylation Reagents-Ketenes ? Stille Coupling ? Substitution and Elimination Reactions of Alkyl Halides ? Suzuki Coupling ? Swern Oxidation ? Ugi Reaction ? Vilsmeier-Haack Reaction
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