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Chemical Structure| 6336-44-3 Chemical Structure| 6336-44-3

Structure of 6336-44-3

Chemical Structure| 6336-44-3

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Product Details of [ 6336-44-3 ]

CAS No. :6336-44-3
Formula : C3H7BO2
M.W : 85.90
SMILES Code : C/C=C/B(O)O
MDL No. :N/A

Safety of [ 6336-44-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 6336-44-3 ]

* 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 [ 6336-44-3 ]

[ 6336-44-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 6336-44-3 ]
  • [ 3998-88-7 ]
  • [ 1122089-24-0 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; triphenylphosphine;tetrakis(triphenylphosphine) palladium(0); In 1,2-dimethoxyethane; water; at 100℃; for 15h; b) To a solution of <strong>[3998-88-7]2-chloro-6-methylisonicotinic acid ethyl ester</strong> (2.0 g, 10.0 mmol), and trans-propenyl boronic acid (1.30 g, 15.13 mmol) in DME (20 mL), a solution of 2 M aq.K2CO3 (3 mL) followed by Pd(PPh3)4 (150 mg, 0.205 mmol) and PPh3 (265 mg, 0.99 mmol) is added. The mixture is stirred at 1000C for 15 h before it is cooled to rt, diluted with ether and washed with sat. aq. Na2CO3 (2x30 mL). The org. extract is dried over Na2SO4, filtered and evaporated. The crude product is purified by CC on silica gel eluting with heptane:EA 4:1 to give 2-propenyl-6-methylisonicotinic acid ethyl ester (2.25 g) as a colourless oil; LC- MS: tR =0.65 min, [M+1]+ = 206.33.
With potassium carbonate;tetrakis(triphenylphosphine) palladium(0); triphenylphosphine; In 1,2-dimethoxyethane; water; at 100℃; for 15h; To a solution of <strong>[3998-88-7]2-chloro-6-methylisonicotinic acid ethyl ester</strong> (2.0 g, 10.0 mmol), and trans-propenyl boronic acid (1.30 g, 15.13 mmol) in DME (20 ml_), a solution of 2 M aq. K2CO3 (3 ml_) followed by Pd(PPh3)4 (150 mg, 0.205 mmol) and triphenylphosphine (265 mg, 0.99 mmol) is added. The mixture is stirred at 100C for 15 h before it is cooled to rt, diluted with diethyl ether and washed with sat. aq. Na2CO3 (2x30 ml_). The org. extract is dried over Na2SO4, filtered and evaporated. The crude product is purified by CC on silica gel eluting with heptane:EA 4:1 to give 2-propenyl-6-methylisonicotinic acid ethyl ester (2.25 g) as a colourless oil; LC-MS: tR =0.65 min, [M+1]+ = 206.33.
With potassium carbonate;tetrakis(triphenylphosphine) palladium(0); triphenylphosphine; In 1,2-dimethoxyethane; water; at 100℃; for 15h; To a solution of <strong>[3998-88-7]2-chloro-6-methylisonicotinic acid ethyl ester</strong> (2.0 g, 10.0 mmol), and trans-propenyl boronic acid (1.30 g, 15.13 mmol) in DME (20 mL), a solution of 2 M aq. K2CO3 (3 mL) followed by Pd(PPh3)4 (150 mg, 0.205 mmol) and PPh3 (265 mg, 0.99 mmol) is added. The mixture is stirred at 100 C. for 15 h before it is cooled to rt, diluted with ether and washed with sat. aq. Na2CO3 (2×30 mL). The org. extract is dried over Na2SO4, filtered and evaporated. The crude product is purified by CC on silica gel eluting with heptane:EA 4:1 to give 2-propenyl-6-methylisonicotinic acid ethyl ester (2.25 g) as a colourless oil; LC-MS: tR=0.65 min, [M+1]+=206.33.
With potassium carbonate; triphenylphosphine;tetrakis(triphenylphosphine) palladium(0); In 1,2-dimethoxyethane; water; at 100℃; for 15h; b) To a solution of <strong>[3998-88-7]2-chloro-6-methylisonicotinic acid ethyl ester</strong> (2.0 g, 10.0 mmol), and trans-propenyl boronic acid (1.30 g, 15.13 mmol) in DME (20 mL), a solution of 2 M aq. K2CO3 (3 mL) followed by Pd(PPh3)4 (150 mg, 0.205 mmol) and triphenylphosphine (265 mg, 0.99 mmol) is added. The mixture is stirred at 100 C. for 15 h before it is cooled to rt, diluted with diethyl ether and washed with sat. aq. Na2CO3 (2*30 mL). The org. extract is dried over Na2SO4, filtered and evaporated. The crude product is purified by CC on silica gel eluting with heptane:EA 4:1 to give 2-propenyl-6-methylisonicotinic acid ethyl ester (2.25 g) as a colourless oil; LC-MS: tR=0.65 min, [M+1]+=206.33.

  • 2
  • [ 76-09-5 ]
  • [ 6336-44-3 ]
  • [ 72824-04-5 ]
 

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