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Chemical Structure| 727985-37-7 Chemical Structure| 727985-37-7

Structure of 727985-37-7

Chemical Structure| 727985-37-7

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Product Details of [ 727985-37-7 ]

CAS No. :727985-37-7
Formula : C8H9BrO
M.W : 201.06
SMILES Code : OCC1=CC(C)=CC=C1Br
MDL No. :MFCD11847170
InChI Key :OWPARZXOXYSXQB-UHFFFAOYSA-N
Pubchem ID :54173415

Safety of [ 727985-37-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 727985-37-7 ]

* 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 [ 727985-37-7 ]

[ 727985-37-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6967-82-4 ]
  • [ 727985-37-7 ]
YieldReaction ConditionsOperation in experiment
79% With lithium aluminium tetrahydride; In tetrahydrofuran; at 0℃;Inert atmosphere; Reflux; PREPARATION 143 (2-Bromo-5-methylphenyl)methanol Lithium aluminium hydride (2.83 g, 74.57 mmol) was suspended in 1 10 ml tetrahydrofuran under nitrogen and cooled to 0 C with an ice-bath. A solution of 2- bromo-5-methylbenzoic acid (6.6 g, 30.69 mmol) dissolved in 60 ml tetrahydrofuran was added drop-wise with stirring. The mixture was then stirred at reflux overnight. The mixture was allowed to cool to room temperature and was quenched by the successive addition with stirring of 3 ml water dissolved in 20 ml tetrahydrofuran, 3 ml 1 N sodium hydroxide and 24 ml water. The mixture was stirred at room temperature overnight. The mixture was filtered through Celite, washing the Celite with ethyl acetate. The combined filtrate was evaporated under reduced pressure and the residue was purified using the Isolera Purification system (ether-hexane gradient, 0: 100 rising to 60:40) to give 4.87g (24.3 mmol, 79%) of the title compound as a white solid. Purity 100%. 1 H N MR (400 MHz, CH LOROFORM-d) delta ppm 2.32 (s, 3 H), 4.71 (d, J=5.47 Hz, 2 H), 6.98 (dd, J=8.01 , 1 .76 Hz, 1 H), 7.28 (s, 1 H), 7.41 (d, J=8.21 Hz, 1 H). UPLC/MS (3 min) retention time 1 .48 min. LRMS: m/z : Molecular ion not detected.
With borane-THF; In tetrahydrofuran; at 0 - 20℃; for 18.5h; A solution of borane THF complex 1M in THF (13.95 mL, 13.95 mmol) was added dropwise to a solution of <strong>[6967-82-4]2-bromo-5-methylbenzoic acid</strong> (1 g, 4.65 mmol) in THF (20 mL) at 000. The resulting mixture was stirred for 30 mm at 0C then allowed to warm to room temperatureand stirred for 18h. The reaction was quenched with methanol followed by 2M hydrochloric acid. The resulting mixture was stirred for 30 mm and extracted with ethyl acetate (3x25 mL). The combined organic solutions were washed with water (25 mL), brine (25 mL), dried over magnesium sulfate, filtered and concentrated in vacuo to the title compound as a white solid; LC MS Rt 1.13 mm; MS mlz [M-18+H] 183.1, 185.1, Method 2minLowpHvo3.
 

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