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Chemical Structure| 795-18-6 Chemical Structure| 795-18-6

Structure of 795-18-6

Chemical Structure| 795-18-6

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Product Details of [ 795-18-6 ]

CAS No. :795-18-6
Formula : C16H23NO4
M.W : 293.36
SMILES Code : O=C(OCC)CCN(CC1=CC=CC=C1)CC(OCC)=O
MDL No. :MFCD09833363

Safety of [ 795-18-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 795-18-6 ]

* 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 [ 795-18-6 ]

[ 795-18-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 795-18-6 ]
  • [ 1027-35-6 ]
YieldReaction ConditionsOperation in experiment
98% With potassium tert-butylate; In toluene; for 2h;Cooling with ice; The crude 1127.324 g compound (c) is dissolved in 2.5 L toluene without water, 243.028g tert potassium butanolate is added gradually under ice bath, stirred for 2h, TLC was carried out to detect the completion of the reaction, 4M HCl in ice bath was added, PH in acidic was adjusted to PH=8 using saturated sodium bicarbonate, extracted with ethyl acetate, dried using anhydrous Na2SO4, filtered, and spin-dried to obtain 376.7g pink solid compound (d), yield 98percent.
78% With potassium tert-butylate; In toluene; at 0℃; for 2h; Above-prepared ethyl 3-[N-benzyl-N-(ethoxycarbonylmethyl)amino]propionate (14.0 g, 0.0479 mol) was dissolved in toluene (100 mL), and the solution was mixed with potassium tert-butoxide (5.9 g, 0.0525 mol) gradually added under ice-cooling, followed by stirring under ice-cooling for two hours. The reaction mixture was mixed with diluted hydrochloric acid (about 1 mol/L, 100 mL) under ice-cooling, followed by shaking and separation, to yield an aqueous layer. Saturated aqueous sodium bicarbonate solution (300 mL) was added dropwise to the aqueous layer, and ethyl acetate (400 mL) was further added thereto, followed by shaking and separation. After drying the organic layer over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure, to thereby yield ethyl 1-benzyl-4-oxopyrrolidine-3-carboxylate (9.23 g, in a yield of 78percent).
 

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