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(S)-7-Benzyloxy-1-(3-benzyloxy-4-methoxy-benzyl)-6-methoxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid ethyl ester

Base Information Edit
  • Chemical Name:(S)-7-Benzyloxy-1-(3-benzyloxy-4-methoxy-benzyl)-6-methoxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid ethyl ester
  • CAS No.:23523-84-4
  • Molecular Formula:C35H37NO6
  • Molecular Weight:567.682
  • Hs Code.:
  • Mol file:23523-84-4.mol
(S)-7-Benzyloxy-1-(3-benzyloxy-4-methoxy-benzyl)-6-methoxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid ethyl ester

Synonyms:

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Chemical Property of (S)-7-Benzyloxy-1-(3-benzyloxy-4-methoxy-benzyl)-6-methoxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid ethyl ester Edit
Chemical Property:
Purity/Quality:
Safty Information:
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MSDS Files:
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Technology Process of (S)-7-Benzyloxy-1-(3-benzyloxy-4-methoxy-benzyl)-6-methoxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid ethyl ester

There total 13 articles about (S)-7-Benzyloxy-1-(3-benzyloxy-4-methoxy-benzyl)-6-methoxy-3,4-dihydro-1H-isoquinoline-2-carboxylic acid ethyl ester 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:
Multi-step reaction with 6 steps
1: 75 percent / KOH / H2O / 5 h / Heating
2: 93 percent / NaBH4 / ethanol / 1.) room temperature, 18 h, 2.) reflux, 1 h
3: 96 percent / PBr3 / tetrahydrofuran / 1.5 h / 0 °C
4: t-BuLi / 1.) THF, hexane, -78 deg C, 30 min, 2.) -100 deg C, 4 h
5: hydrazine, acetic acid / ethanol; H2O / 2 h / Ambient temperature
6: K2CO3 / acetone / 14 h / Heating
With potassium hydroxide; sodium tetrahydroborate; tert.-butyl lithium; phosphorus tribromide; potassium carbonate; acetic acid; hydrazine; In tetrahydrofuran; ethanol; water; acetone;
Guidance literature:
Multi-step reaction with 6 steps
1: 75 percent / KOH / H2O / 5 h / Heating
2: 93 percent / NaBH4 / ethanol / 1.) room temperature, 18 h, 2.) reflux, 1 h
3: 96 percent / PBr3 / tetrahydrofuran / 1.5 h / 0 °C
4: t-BuLi / 1.) THF, hexane, -78 deg C, 30 min, 2.) -100 deg C, 4 h
5: hydrazine, acetic acid / ethanol; H2O / 2 h / Ambient temperature
6: K2CO3 / acetone / 14 h / Heating
With potassium hydroxide; sodium tetrahydroborate; tert.-butyl lithium; phosphorus tribromide; potassium carbonate; acetic acid; hydrazine; In tetrahydrofuran; ethanol; water; acetone;
Guidance literature:
Multi-step reaction with 7 steps
1: 73 percent / ammonium acetate / 1.5 h / Heating
2: 55 percent / lithium aluminum hydride / diethyl ether; tetrahydrofuran / 1.) reflux, 2 h, 2.) room temperature, overnight
3: formic acid / 48 h / 50 °C
4: 88 percent / ammonium sulfate / toluene / 48 h / Heating
5: t-BuLi / 1.) THF, hexane, -78 deg C, 30 min, 2.) -100 deg C, 4 h
6: hydrazine, acetic acid / ethanol; H2O / 2 h / Ambient temperature
7: K2CO3 / acetone / 14 h / Heating
With ammonium acetate; ammonium sulfate; lithium aluminium tetrahydride; tert.-butyl lithium; potassium carbonate; acetic acid; hydrazine; In tetrahydrofuran; formic acid; diethyl ether; ethanol; water; acetone; toluene;
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