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Chemical Structure| 253429-08-2 Chemical Structure| 253429-08-2

Structure of 253429-08-2

Chemical Structure| 253429-08-2

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Product Details of [ 253429-08-2 ]

CAS No. :253429-08-2
Formula : C10H19NO2
M.W : 185.26
SMILES Code : O=C(C1CCCCCC1)N(OC)C
MDL No. :MFCD12546238

Safety of [ 253429-08-2 ]

Application In Synthesis of [ 253429-08-2 ]

* 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 [ 253429-08-2 ]

[ 253429-08-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 6557-86-4 ]
  • [ 6638-79-5 ]
  • [ 253429-08-2 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In dichloromethane; N,O-dimethylhydroxylamine hydrochloride (18.03 g, 0.185 mol) was suspended in methylene chloride (200 mL) and treated with triethylamine (49.1 mL, 0.35 mol). The mixture was stirred for 15 minutes at room temperature and then cooled to 0 C. The above-formed <strong>[6557-86-4]acid chloride of cycloheptanecarboxylic acid</strong> dissolved in methylene chloride (30 mL) was added dropwise to the cooled solution. After addition was complete, the reaction mixture was warmed to room temperature and allowed to stir for 17 hours. The mixture was then poured into water (200 mL). The layers were separated, and the organic layer was dried over anhydrous sodium sulfate, filtered and concentrated to provide N-methoxy-N-methyl cycloheptyl amide.
With triethylamine; In dichloromethane; N,O-dimethylhydroxylamine hydrochloride (18.03 g, 0.185 mol) was suspended in methylene chloride (200 mL) and treated with triethylamine (49.1 mL, 0.35 mol). The mixture was stirred for 15 minutes at room temperature and then cooled to 0 C. The above-formed <strong>[6557-86-4]acid chloride of cycloheptanecarboxylic acid</strong> dissolved in methylene chloride (30 mL) was added dropwise to the cooled solution. After addition was complete, the reaction mixture was warmed to room temperature and allowed to stir for 17 hours. The mixture was then poured into water (200 mL). The layers were separated, and the organic layer was dried over anhydrous sodium sulfate, filtered and concentrated to provide N-methoxy-N-methyl cycloheptyl amide.
N,O-dimethylhydroxylamine hydrochloride (18.03 g, 0.185 mol) was suspended in methylene chloride (200 mL) and treated with triethylamine (49.1 mL, 0.35 mol). The mixture was stirred for 15 minutes at room temperature and then cooled to 0 C. The above-formed <strong>[6557-86-4]acid chloride of cycloheptanecarboxylic acid</strong> dissolved in methylene chloride (30 mL) was added dropwise to the cooled solution. After addition was complete, the reaction mixture was warmed to room temperature and allowed to stir for 17 hours. The mixture was then poured into water (200 mL). The layers were separated, and the organic layer was dried over anhydrous sodium sulfate, filtered and concentrated to provide N-methoxy-N-methyl cycloheptyl amide.
Cycloheptanecarboxylic acid (25.0 g, 0.176 mol) was dissolved in methylene chloride (100 mL) and oxalyl chloride (23 mL, 0.264 mol) was added dropwise to the solution. The reaction mixture was stirred for 30 minutes at room temperature and then concentrated under vacuum to provide the <strong>[6557-86-4]acid chloride of cycloheptanecarboxylic acid</strong> as a yellow oil. [00124] N,O-dimethylhydroxylamine hydrochloride (18.03 g, 0.185 mol) was suspended in methylene chloride (200 mL) and treated with triethylamine (49.1 mL, 0.35 mol). The mixture was stirred for 15 minutes at room temperature and then cooled to 0 C. The above-formed <strong>[6557-86-4]acid chloride of cycloheptanecarboxylic acid</strong> dissolved in methylene chloride (30 mL) was added dropwise to the cooled solution. After addition was complete, the reaction mixture was warmed to room temperature and allowed to stir for 17 hours. The mixture was then poured into water (200 mL). The layers were separated, and the organic layer was dried over anhydrous sodium sulfate, filtered and concentrated to provide N-methoxy-N-methyl cycloheptyl amide.
With triethylamine; In dichloromethane; at 0 - 20℃; for 17h; N,O-dimethylhydroxylamine hydrochloride (18.03 g, 0.185 mol) was suspended in methylene chloride (200 mL) and treated with triethylamine (49.1 mL, 0.35 mol). The mixture was stirred for.15 minutes at room temperature and then cooled to 0 C. The above-formed <strong>[6557-86-4]acid chloride of cycloheptanecarboxylic acid</strong> dissolved in methylene chloride (30 mL) was added dropwise to the cooled solution. After addition was complete, the reaction mixture was warmed to room temperature and allowed to stir for 17 hours. The mixture was then poured into water (200 mL). The layers were separated, and the organic layer was dried over anhydrous sodium sulfate, filtered and concentrated to provide N-methoxy-N-methyl cycloheptyl amide.

 

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