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Chemical Structure| 947163-26-0 Chemical Structure| 947163-26-0

Structure of 947163-26-0

Chemical Structure| 947163-26-0

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Product Details of [ 947163-26-0 ]

CAS No. :947163-26-0
Formula : C8H9BO3
M.W : 163.97
SMILES Code : OB1OCC2=CC=C(OC)C=C12
MDL No. :MFCD16658744
InChI Key :GAGAFKOBUXAXBW-UHFFFAOYSA-N
Pubchem ID :52919292

Safety of [ 947163-26-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 947163-26-0 ]

* 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 [ 947163-26-0 ]

[ 947163-26-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 947163-26-0 ]
  • [ 1196473-37-6 ]
YieldReaction ConditionsOperation in experiment
99.6% With boron tribromide; In dichloromethane; at -10 - 20℃; To a solution of 19 (10.0 g, 61.0 mmol) in dichloromethane (400 mL) was slowly added BBr3 (134 mL, 1 M in DCM, 0.134 mol) at -10 to -5 °C. The mixture was stirred at 0 °C to room temperature for 3 h. The reaction mixture was poured into ice-water (300 mL). The resulting mixture was extract with EtOAc (600 mL). The extract was washed with brine, dried and concentrated to dryness to give 9.11 g (99.6percent) of 20 as off-white foam.
99.6% With boron tribromide; In dichloromethane; at -10 - 20℃; To a solution of 6-methoxy-3H-benzo[c][1,2]oxaborol-1-ol (10.0 g, 61.0 mmol) in dichloromethane (400 mL) was slowly added boron tribromide (134 mL, 1 M in DCM, 0.134 mol) at -10 to -5° C. The mixture was stirred at 0° C. to room temperature for 3 h. The reaction mixture was poured into ice-water (300 mL). The resulting mixture was extract with EtOAc (600 mL). The extract was washed with brine, dried and concentrated to dryness to give 9.11 g (99.6percent yield) of product as off-white foam. 1H NMR (400 MHz, DMSO-d6) delta 9.27 (br. s., 1H), 9.03 (br. s., 1H), 7.16 (d, J=8.20 Hz, 1H), 7.08 (d, J=2.34 Hz, 1H), 6.86 (dd, J=8.20, 2.34 Hz, 1H). MS (ESI) m/z=151 [M+H]+.
2 g With boron tribromide; In dichloromethane; at -30 - 20℃; for 3h; Step 3: Intermediate 5-16b (2.500 g, 15.25 mmol, 1.0 eq) was dissolved in dichloromethane (100 mL) and cooled to -30.A 1 mol/L solution of boron tribromide in dichloromethane (60 mL, 60 mmol, 3.9 eq) was slowly added dropwise, and after completion of dropwise addition, the mixture was slowly warmed to room temperature for 3 hours.After the reaction was completed, the reaction mixture was poured into ice water (200 mL), and the mixture was separated, and the phases were separated. The aqueous phase was extracted with dichloromethane.Saturated brine (50mL), dried over anhydrous sodium sulfate, filtered and the filtrate was concentrated to give intermediate 5-16 total 2.00g.
  • 2
  • [ 1196473-37-6 ]
  • [ 74-88-4 ]
  • [ 947163-26-0 ]
YieldReaction ConditionsOperation in experiment
50% H181 (150 mg, 1.0 mmol) was dissolved in DMF (8.0 mL) and cooled to 0°C with ice bath. To this solution under nitrogen were added in sequence NaH (60percent> in mineral oil, 120 mg, 3.0 mmol) and iodomethane (0.1 mL, 2.0 mmol). The reaction mixture was stirred for 2 h then treated with 1.0 M HC1 (10.0 mL). After extraction with ethyl acetate, the organic phase was washed with water and brine, and dried over anhydrous Na2S04. The residue after rotary evaporation was purified by column chromatography over silica gel to give the title compound (81.9 mg, 50percent yield). 1H NMR (400 MHz, CDC13): delta 7.26 (d, J = 8.4 Hz, 1H), 7.23 (d, J = 2.4 Hz, 1H), 7.07 (dd, J = 8.1 2.4 Hz, 1H), 5.06 (s, 2H) and 3.84 (s, 3H) ppm; Mp: 107-109 °C.
 

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