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Chemical Structure| 1382137-67-8 Chemical Structure| 1382137-67-8

Structure of 1382137-67-8

Chemical Structure| 1382137-67-8

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Product Details of [ 1382137-67-8 ]

CAS No. :1382137-67-8
Formula : C12H22BNO4S
M.W : 287.18
SMILES Code : CC1(C)OB(OC1(C)C)C1=CCN(CC1)S(C)(=O)=O
MDL No. :MFCD28962592
InChI Key :WUYGKJHVVHTRPV-UHFFFAOYSA-N
Pubchem ID :67973497

Safety of [ 1382137-67-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 1382137-67-8 ]

* 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 [ 1382137-67-8 ]

[ 1382137-67-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1121057-75-7 ]
  • [ 124-63-0 ]
  • [ 1382137-67-8 ]
YieldReaction ConditionsOperation in experiment
75% With triethylamine; In dichloromethane; at 20℃; To a mixture of the product from the previous step (4.0 g, 16 mmol) and TEA (6.3 mL, 48 mmol) in CH2Cl2 (60 mL) at RT was added methanesulfonyl chloride (1.5 mL, 20 mmol) dropwise and the reaction was stirred at RT overnight. The reaction mixture was diluted with CH2Cl2 (60 mL), washed with IN HCl to pH = 5, then with brine (50 mL), and then dried over Na2S04, filtered and concentrated under reduced pressure. The residue was washed with petroleum ether (100 mL) to afford the title compound (3.5 g, 75percent yield) as a white solid.MS (ES+) C12H22BNO4S, requires: 287, found 288 [M+H]+.
7.4 g With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20℃; for 12h; Step 2: 1-(Methylsulfonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine To a cooled (0° C.) solution of <strong>[1121057-75-7]4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridinium chloride</strong> (8 g) and N-ethyldiisopropylamine (12 mL) in dichloromethane (100 mL) is added dropwise methanesulfonyl chloride (3 mL). The mixture is stirred for 12 hours at room temperature. The mixture is partitioned between dichloromethane and 0.1 M hydrochloric acid. The organic phase is separated, washed with brine and dried (MgSO4). The solvent is evaporated and the residue is crystallized from diethylether to give the title compound. Yield: 7.4 g; LC (method 15): tR=0.98 min; Mass spectrum (ESI+): m/z=288 [M+H]+.
7.4 g With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20℃; for 12h; To a cooled (0°C) solution of 4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)-1 ,2,3,6- tetrahydropyridinium chloride (8 g) and N-ethyldiisopropylamine (12 mL) in dichloromethane (100 mL) is added dropwise methanesulfonyl chloride (3 mL). The mixture is stirred for 1 2 hours at room temperature. The mixture is partitioned between dichloromethane and 0.1 M hydrochloric acid. The organic phase is separated, washed with brine and dried (MgSO4). The solvent is evaporated and the residue is crystallized from diethylether to give the title compound. Yield: 7.4 g; LC (method 15): tR = 0.98 min; Mass spectrum (ESI+): m/z = 288 [M+H]+.
With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20℃; for 12h; To a cooled (0°C) solution of 4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)-1 ,2,3,6- tetrahydropyridinium chloride (8 g) and N-ethyldiisopropylamine (12 mL) in dichloromethane (100 mL) is added dropwise methanesulfonyl chloride (3 mL). The mixture is stirred for 12 hours at room temperature. The mixture is partitioned between dichloromethane and 0.1 M hydrochloric acid. The organ ic phase is separated, washed with brine and dried (MgSO4). The solvent is evaporated and the residue is crystallized from diethylether to give the title compound. Yield: 7.4 g; LC (method 15): tR = 0.98 min; Mass spectrum (ESI+): m/z = 288 [M+H]+.

 

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