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Chemical Structure| 177036-78-1 Chemical Structure| 177036-78-1

Structure of 177036-78-1

Chemical Structure| 177036-78-1

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Product Details of [ 177036-78-1 ]

CAS No. :177036-78-1
Formula : C17H18O4
M.W : 286.32
SMILES Code : O=C(OC)[C@@H](O)C(C1=CC=CC=C1)(OC)C2=CC=CC=C2
MDL No. :MFCD11865341

Safety of [ 177036-78-1 ]

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

Application In Synthesis of [ 177036-78-1 ]

* 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 [ 177036-78-1 ]

[ 177036-78-1 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 35144-22-0 ]
  • [ 177036-78-1 ]
  • [ 1106685-61-3 ]
YieldReaction ConditionsOperation in experiment
72.96% With potassium carbonate; In N,N-dimethyl-formamide; at 90 - 92℃; for 1h;Inert atmosphere; Example 4:Preparation of (S)-methyl-2-(4,6-dimethylpyrimidin-2-yloxy)-3-methoxy-3,3- diphenylpropionate (compound ??; R' = methyl, R= methyl)To a stirred solution of (S)-methyl-2-hydroxy-3-methoxy-3,3-diphenylpropionate (compound IV; 79 gms/0.276 moles) and potassium carbonate(41.9gms / 0.303moles) in DMF (790 ml) was added 4,6-Dimethyl-2-(methyl sulfonyl) pyrimidine (compound III; R= methyl) (56.5 gms /0.303 moles) in a dry flask under nitrogen at 25-30C. The reaction mass was heated to 90-92C and further stirred for 1 hour. The reaction mass was charged with ethyl acetate (2.4 lit). The organic layer was washed with 2N citric acid (500 ml) followed by water and treated with charcoal. The clear filtrate was distilled completely under vacuum. The residue was stirred with n-heptane (300 ml), filtered and dried to obtain 90 gms of compound (II).The compound (II) was dissolved in acetonitrile (1.8 lit) and isolated in water (4.5 lit). The solid was isolated by filtration and dried to obtain 79 gms of compound (II).Efficiency: 72.96 % Purity by HPLC:99.8%Chiral purity: 99.97%
Example-12: Preparation of (+)-(2S)-2-[(4,6-dimethyIpyrimidin-2-yl)oxy]-3- methoxy-3,3-diphenylpropanoic acid methyl ester compound of formula-lOa:Mixture of (S)-2-hydroxy-3-methoxy-3,3-diphenylpropionic acid methyl ester compound formula-8a (50 grams), dimethyl formamide (500 ml) and potassium carbonate (12 grams) was stirred at 40 minutes at 25-350C. 4,6-dimethyl-2- (methylsulphonyl) pyrimidine (34.5 grams) was added and heated to 90-950C and stirred for 4 hours. The reaction mixture was cooled to 25-35C. Water (250 ml) was added and stirred for 60 minutes. The solid obtained was filtered, washed with water and then dried at 60-700C to get the title compound. Yield: 55 grams M.R: 130-1400C; S.O.R: +135.8 (C= 0.5; MeOH)
Preparation of (+)-(2S)-2-[(4,6-dimethylpyrimidin-2-yl)oxy]-3-methoxy-3,3-diphenylpropanoic acid methyl ester compound of formula-10a Mixture of (S)-2-hydroxy-3-methoxy-3,3-diphenylpropionic acid methyl ester compound formula-8a (50 grams), dimethyl formamide (500 ml) and potassium carbonate (12 grams) was stirred at 40 minutes at 25-35 C. 4,6-dimethyl-2-(methylsulphonyl)pyrimidine (34.5 grams) was added and heated to 90-95 C. and stirred for 4 hours. The reaction mixture was cooled to 25-35 C. Water (250 ml) was added and stirred for 60 minutes. The solid obtained was filtered, washed with water and then dried at 60-70 C. to get the title compound.Yield: 55 gramsM.R: 130-140 C.;S.O.R: +135.8 (C=0.5; MeOH)
  • 2
  • [ 178306-47-3 ]
  • [ 177036-78-1 ]
  • 3
  • [ 110-78-1 ]
  • [ 178306-47-3 ]
  • [ 1349685-28-4 ]
  • [ 1349685-29-5 ]
  • (-)-methyl 3-methoxy-3,3-diphenyl-2-propylaminocarbonyloxypropanoate [ No CAS ]
  • [ 177036-78-1 ]
 

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