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Chemical Structure| 98198-78-8 Chemical Structure| 98198-78-8

Structure of 98198-78-8

Chemical Structure| 98198-78-8

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Product Details of [ 98198-78-8 ]

CAS No. :98198-78-8
Formula : C6H7ClO
M.W : 130.57
SMILES Code : O=C(Cl)C1CC(C1)=C
MDL No. :MFCD08235240

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Application In Synthesis of [ 98198-78-8 ]

* 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 [ 98198-78-8 ]

[ 98198-78-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 15760-36-8 ]
  • [ 98198-78-8 ]
YieldReaction ConditionsOperation in experiment
75% With thionyl chloride; at 90℃; for 3h; Reference Example 2 <strong>[15760-36-8]3-methylenecyclobutanecarboxylic acid</strong> chloride In a 50 mL round-bottom flask equipped with a dropping funnel and water condenser with drying tube, the carboxylic acid prepared above (26.19 g, 0.234 mole) was charged. Thionyl chloride (20.5 mL, 0.281 mole, 1.2 equiv) was added dropwise. The mixture was heated at reflux (oil bath temperature 90 C.) for 3 h then cooled to room temperature. The condenser was replaced with a distillation head and the mixture was distilled under vacuum. A clear colorless liquid was collected at 43-45 C. (23 g, 75% yield). 1H NMR (300 MHz, CDCl3) δ ppm 4.85-4.93 (m, 2H), 3.50-3.63 (m, 1H), 2.95-3.19 (m, 4H).
With oxalyl dichloride;N,N-dimethyl-formamide; In dichloromethane; at 20℃; for 2h; Step 2. N-methoxy-N-methyl-3-methylenecyclobutanecarboxamide To a mixture of <strong>[15760-36-8]3-methylenecyclobutanecarboxylic acid</strong> (Step 1, 5.88 g, 52.4 mmol) in methylene chloride (100 mL) was added oxalyl chloride (Aldrich, 5.33 mL, 62.9 mmol), followed by a catalytic amount of dimethyl formamide (DMF). The reaction was stirred at rt for 2 h, then evaporated to dryness. The crude acid chloride was dissolved in methylene chloride (200 mL). To the resulting solution was added N,O-dimethylhydroxylamine hydrochloride ((Aldrich, 0.14 g, 62.9 mmol), followed by triethylamine (TEA) (21.9 mL, 0.157 mol), dropwsie, at 0 C. The reaction was stirred at rt overnight, and TEA HCl salt was filtered out. The filtrate was washed with 1 N HCl, then aq. sodium bicarbonate, brine, and dried over magnesium sulfate and evaporated to dryness. The crude amide (7.30 g, 89.7%) was used directly in next step. LCMS calculated for C8H14NO2(M+H)+: m/z=156.1; Found: 156.3.
With oxalyl dichloride; In dichloromethane; N,N-dimethyl-formamide; at 20℃; for 4h; To a solution of 3 -methyl enecy cl obutane-1-carboxylic acid (1.22 g, 10.88 mmol) in DCM (9.1 mL) was added DMF (0.042 mL, 0.544 mmol) followed by oxalyl chloride (0.95 mL, 10.88 mmol). The reaction was stirred at RT for 4h.
 

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