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Chemical Structure| 198277-06-4 Chemical Structure| 198277-06-4

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Chemical Structure| 198277-06-4

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Product Details of [ 198277-06-4 ]

CAS No. :198277-06-4
Formula : C8H9BrO2
M.W : 217.06
SMILES Code : OC1=CC=C(Br)C=C1CCO
MDL No. :MFCD09907900

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Application In Synthesis of [ 198277-06-4 ]

* 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 [ 198277-06-4 ]

[ 198277-06-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 7768-28-7 ]
  • [ 198277-06-4 ]
YieldReaction ConditionsOperation in experiment
65% With N-Bromosuccinimide; sulfuric acid; In tetrahydrofuran; at -25 - 20℃; Cone. H2S04 (11 f.LL, 0.20 mmol) and N-bromosuccinimide (779 mg, 4.38 mmol) were added to a solutionof 2-(2-hydroxyethyl)phenol (550 mg, 3.98 mmol) in THF(7 mL) at -25° C. The mixture was allowed to warm tort andstirred overnight. Aq. sodium thiosulfite (10percent aq. solution,10 mL) and water (5 mL) were added and the resultingmixture was extracted with EtOAc (2x50 mL). The combinedorganic layers were washed with brine (10 mL), driedover MgS04 , and concentrated in vacuo. The crude productwas chromatographed (Si02 ; 40 g; continuous gradient from0 to 40percent Solvent B over 35 min, hold at 40percent Solvent B for10 min, where Solvent A=hexanes and Solvent B=EtOAc) togive the title compound (558 mg, 2.57 mmol, 65percent yield) asa beige solid. 1H NMR (500 MHz, CDCI3 d) o7.91 (s, lH),7.27-7.23 (m, lH), 7.19 (d, 1=2.5 Hz, lH), 6.81 (d, 1=8.5 Hz,lH), 4.01 (td, 1=5.2, 3.4 Hz, 2H), 2.89-2.85 (m, 2H), 2.28 (t,1=3.2 Hz, lH).
With N-Bromosuccinimide; sulfuric acid; In tetrahydrofuran; at -25 - 25℃; Example 53i 4-Bromo-2-(2-hydroxy-ethyl)-phenol Concentrated H2SO4 (0.7 mL, 12.7 mmol) and NBS (49.6 g, 278.6 mmol) were added to a solution of 2-hydroxyphenethyl alcohol (35.0 g, 253.3 mmol) in dry THF (500 mL) at -25° C. The mixture was allowed to warm to room temperature and stirred overnight. Aqueous sodium thiosulfite (10percent, 70 mL) and water (200 ml) were added and the resulting mixture was extracted with ethyl acetate (2*400 mL). The combined organic extracts were washed with brine, dried over sodium sulfate and concentrated under reduced pressure. The residue was purified by flash column chromatography using 50percent ethyl acetate in hexane to afford 55.0 g of the title compound: 1H NMR (400 MHz, CDCl3) delta ppm 8.03 (br, s, OH), 7.25-7.22 (m, 1H), 7.18 (m, 1H), 6.80 (d, 1H), 3.99 (t, 2H), 2.85 (t, 2H), 2.50 (br, s, OH).
With N-Bromosuccinimide; sulfuric acid; In tetrahydrofuran; at -25℃; for 1h; EXAMPLE 74; Preparation of: 2-amino-5-[4-(difluoromethoxy)-3-(2-fluoroethyl)phenyl]-3-methyl-5-phenyl-3,5- dihydro-4H-imidazol-4-oneStep 1 :4-bromo-2-(2-hvdroxyethyl)phenolIn a 1 L round-bottomed flask was placed 2-(2-hydroxyethyl)phenol (50 g, 362 mmol) and THF (724 mL) was added to give a brown solution. The reaction was cooled to-25 0C.Sulfuric acid (0.964 mL, 18.09 mmol) was added. N-Bromosuccinimide (70.9 g, 398 mmol) was added and reaction stirred for 1h at -25 0C and then allowed to warm to RT overnight. A 10percent sodium thiosulfite solution was added (100 mL). EtOAc (500 mL) was added and the organic was washed with water (2 x 200 mL) and brine (200 mL). The organic layer was dried over Na2SO4. The crude material was purified by flash chromatography (0-100percent EtOAc/hex) to provide the desired product in quantitative yield and used directly in subsequent reaction. 1H NMR (400 MHz, DMSO-d6) delta 9.60 (s, 1H), 7.20 (s, 1 H), 7.15 (d, J = 8.0 Hz, 1 H), 6.71 (d, J = 8.0 Hz, 1 H), 4.65 (b, 1 H), 3.55 (t, J = 6.8 Hz, 2H)1 2.64 (t, J = 7.0 Hz, 2H)
 

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