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3-((4S,trans)-4,5-dihydro-4-methyl-2-phenyloxazol-5-yl)-N-methoxy-N-methyl propionamide

Base Information Edit
  • Chemical Name:3-((4S,trans)-4,5-dihydro-4-methyl-2-phenyloxazol-5-yl)-N-methoxy-N-methyl propionamide
  • CAS No.:503560-09-6
  • Molecular Formula:C15H20N2O3
  • Molecular Weight:276.335
  • Hs Code.:
  • Mol file:503560-09-6.mol
3-((4S,trans)-4,5-dihydro-4-methyl-2-phenyloxazol-5-yl)-N-methoxy-N-methyl propionamide

Synonyms:3-((4S,trans)-4,5-dihydro-4-methyl-2-phenyloxazol-5-yl)-N-methoxy-N-methyl propionamide

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 3-((4S,trans)-4,5-dihydro-4-methyl-2-phenyloxazol-5-yl)-N-methoxy-N-methyl propionamide Edit
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Technology Process of 3-((4S,trans)-4,5-dihydro-4-methyl-2-phenyloxazol-5-yl)-N-methoxy-N-methyl propionamide

There total 12 articles about 3-((4S,trans)-4,5-dihydro-4-methyl-2-phenyloxazol-5-yl)-N-methoxy-N-methyl propionamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In methanol; benzene; for 1h; Heating;
DOI:10.1016/S0957-4166(02)00794-2
Guidance literature:
Multi-step reaction with 8 steps
1.1: O3 / methanol / -78 °C
2.1: LiCl; DBU / acetonitrile / 1 h
2.2: 2.03 g / acetonitrile / 2 h
3.1: 82.4 percent / CuBr; Red-Al; 2-butanol / tetrahydrofuran / 4 h / -20 °C
4.1: aq. LiOH / tetrahydrofuran / 2 h
5.1: 491 mg / Et3N; DCC; HOBt / CH2Cl2 / 12 h
6.1: 94 percent / TBAF / tetrahydrofuran / 1 h / 20 °C
7.1: 90 percent / PPh3; imidazole; I2 / acetonitrile; diethyl ether / 4 h / 20 °C
8.1: 87.5 percent / AIBN; Bu3SnH / benzene; methanol / 1 h / Heating
With 1H-imidazole; lithium hydroxide; 2,2'-azobis(isobutyronitrile); tetrabutyl ammonium fluoride; iodine; tri-n-butyl-tin hydride; benzotriazol-1-ol; ozone; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; dicyclohexyl-carbodiimide; triphenylphosphine; sodium bis(2-methoxyethoxy)aluminium dihydride; iso-butanol; lithium chloride; copper(I) bromide; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; acetonitrile; benzene;
DOI:10.1016/S0957-4166(02)00794-2
Guidance literature:
Multi-step reaction with 11 steps
1.1: 96 percent / tetrahydrofuran / 1 h / -78 °C
2.1: 99 percent / pyridine / CH2Cl2 / 12 h
3.1: 75 percent / K2CO3; Pd(PPh3)4 / acetonitrile / 24 h / Heating
4.1: O3 / methanol / -78 °C
5.1: LiCl; DBU / acetonitrile / 1 h
5.2: 2.03 g / acetonitrile / 2 h
6.1: 82.4 percent / CuBr; Red-Al; 2-butanol / tetrahydrofuran / 4 h / -20 °C
7.1: aq. LiOH / tetrahydrofuran / 2 h
8.1: 491 mg / Et3N; DCC; HOBt / CH2Cl2 / 12 h
9.1: 94 percent / TBAF / tetrahydrofuran / 1 h / 20 °C
10.1: 90 percent / PPh3; imidazole; I2 / acetonitrile; diethyl ether / 4 h / 20 °C
11.1: 87.5 percent / AIBN; Bu3SnH / benzene; methanol / 1 h / Heating
With pyridine; 1H-imidazole; lithium hydroxide; tetrakis(triphenylphosphine) palladium(0); 2,2'-azobis(isobutyronitrile); tetrabutyl ammonium fluoride; iodine; tri-n-butyl-tin hydride; potassium carbonate; benzotriazol-1-ol; ozone; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; dicyclohexyl-carbodiimide; triphenylphosphine; sodium bis(2-methoxyethoxy)aluminium dihydride; iso-butanol; lithium chloride; copper(I) bromide; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; acetonitrile; benzene;
DOI:10.1016/S0957-4166(02)00794-2
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