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Chemical Structure| 150884-50-7 Chemical Structure| 150884-50-7

Structure of 150884-50-7

Chemical Structure| 150884-50-7

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Product Details of [ 150884-50-7 ]

CAS No. :150884-50-7
Formula : C12H15NO2
M.W : 205.25
SMILES Code : O=C(OC(C)(C)C)/N=C/C1=CC=CC=C1
MDL No. :MFCD11041300
InChI Key :XFRQMBFCAKTYIV-UHFFFAOYSA-N
Pubchem ID :57109745

Safety of [ 150884-50-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H317-H319-H335
Precautionary Statements:P261-P280-P305+P351+P338

Application In Synthesis of [ 150884-50-7 ]

* 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 [ 150884-50-7 ]

[ 150884-50-7 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 75-07-0 ]
  • [ 150884-50-7 ]
  • [ 135865-78-0 ]
YieldReaction ConditionsOperation in experiment
55% With L-proline; In acetonitrile; at 0℃; for 3h; To a stirred solution of aryl N-Boc benzalimine 6 (5 g, 24 mmol) in CH3CN (41 mL) and 0.74 M redistilled acetaldehyde (7.2 mL, 120 mmol) in CH3CN (135 mL) at 0 C was added L-proline (552 mg, 20 mol%) as the case may be and the mixture stirred further at 0 C for 3 h. After the completion of reaction (monitored by TLC), it was quenched with water and extracted with Et2O (3 x 50 mL). The combined organic layers were washed with brine, dried over anhyd. Na2SO4, filtered and concentrated under reduced pressure to give the crude aldehyde. Flash column chromatographic purification [silica gel (230-400 mesh) and pet. ether: EtOAc(80:20) as an eluent] gave beta-aminoaldehyde (-)-5.
55% With L-proline; In acetonitrile; at 0℃; for 3h; General procedure: EXAMPLE 1 General experimental procedure for the synthesis of (+)-sertraline (i) (S)-tert-Butyl (3-oxo-l-phenylpropyl)carbamate To a stirred solution of aryl N-Boc-imine (1.4 mmol) and redistilled acetaldehyde (0.39 mL, 7 mmol) in CH3CN (15 mL) at 0 C was added L-proline (0.032 g, 20 mol%) and the mixture stirred further at 0 C for 3 h. After the completion of reaction (monitored by TLC), it was quenched with water and extracted with Et20 (3 x 50 mL). The combined organic layers were washed with brine, dried over anhyd. Na2S04, filtered and concentrated under reduced pressure to give the crude aldehyde. Flash column chromatographic purification [silica gel (230-400 mesh) and pet. ethenEtOAc as an eluent] gave beta- aminoaldehyde. Yield: 55%; pale yellow solid; mp: 91-94 C, (lit.33 mp: 92-93.5 C); [a]D25 -30.10 (c 1.15, CHC13); lit.33 [a]D25 +29.0 (c 1.4, CHC13) for its antipode; IR (CHC13, cm"1): umax 700, 1021, 1049, 1169, 1250, 1369, 1391, 1498, 1513, 1692, 2977, 3341; 1H NMR (200 MHz, CDC13): delta 1.41 (s, 9H), 2.83-2.96 (m, 2H), 4.87 (br s, 1H), 5.17 (br s, 1H), 7.26-7.34 (m, 5H), 9.73 (t, J = 1.7 Hz, 1H); 13C NMR (50 MHz, CDC13): delta 28.3, 39.9, 49.9, 79.9, 126.3, 127.7, 128.8, 135.2, 155.0, 193.3, 199.8; Analysis: Ci4H19N03 requires C, 67.45; H, 7.68; N, 5.62; found: C, 67.32; H, 7.41; N, 5.46%.
52% L-proline; In acetonitrile; at 0℃; for 4h; The N-Boc imine (287.4 mg, 1.4 mmol) was dissolved in 9.5 ml of a 0.74M solution of acetaldehyde (5 eq.) in dry acetonitrile, cooled to 0 C. and then admixed with (L)-proline (32.2 mg, 0.28 mmol, 20 mol %). After 4 h at 0 C., the reaction mixture was added to water and extracted three times with diethyl ether. The combined organic phases were washed once with saturated aqueous sodium chloride solution and dried over-MgSO4. The product was purified by column chromatography on silica gel using ethyl acetate/hexane (first 10/90, then 20/80, vol/vol) as the eluent. The product is obtained in 52% yield. The enantiomeric ratio of the product was determined by means of gas chromatography to be >99:1.
  • 2
  • [ 135865-78-0 ]
  • [ 150884-50-7 ]
  • tert-butyl-(1R,2R,3S)2-formyl-1,3-diphenylpropane-1,3-diyldicarbamate [ No CAS ]
  • 3
  • [ 75-07-0 ]
  • [ 150884-50-7 ]
  • [ 479423-39-7 ]
  • [ 1027769-25-0 ]
  • [ 1152166-54-5 ]
  • [ 1152166-55-6 ]
  • C27H38N2O5 [ No CAS ]
  • [ 135865-78-0 ]
  • 4
  • [ 135865-78-0 ]
  • [ 150884-50-7 ]
  • [ 1152166-54-5 ]
  • 6
  • [ 2840-44-0 ]
  • [ 150884-50-7 ]
  • tert-butyl ((S)-((R)-7-fluoro-1-oxo-1,2,3,4-tetrahydronaphthalen-2-yl)(phenyl)methyl)carbamate [ No CAS ]
 

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