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(R)-5-Benzyloxy-4-hydroxy-2-(3-methoxy-phenyl)-pentanenitrile

Base Information Edit
  • Chemical Name:(R)-5-Benzyloxy-4-hydroxy-2-(3-methoxy-phenyl)-pentanenitrile
  • CAS No.:83287-36-9
  • Molecular Formula:C19H21NO3
  • Molecular Weight:311.381
  • Hs Code.:
  • Mol file:83287-36-9.mol
(R)-5-Benzyloxy-4-hydroxy-2-(3-methoxy-phenyl)-pentanenitrile

Synonyms:

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (R)-5-Benzyloxy-4-hydroxy-2-(3-methoxy-phenyl)-pentanenitrile Edit
Chemical Property:
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Technology Process of (R)-5-Benzyloxy-4-hydroxy-2-(3-methoxy-phenyl)-pentanenitrile

There total 1 articles about (R)-5-Benzyloxy-4-hydroxy-2-(3-methoxy-phenyl)-pentanenitrile 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 lithium diisopropyl amide; In tetrahydrofuran; 1.) -78 deg C; 2.) to room temperature;
DOI:10.1248/cpb.30.2641
Guidance literature:
Multi-step reaction with 9 steps
1: potassium hydroxide / ethanol / 7 h / Heating
2: 80 percent / LDA / tetrahydrofuran / 1.) -78 deg C; 2.) to room temperature
3: hydrogen, trace of perchloric acid / 10percent palladized charcoal / methanol
4: 1.) methanolic potassium hydroxide; 2.) sodium periodate; 3.) sodium borohydride
5: 82 percent / H2O / 12 h / 180 °C / in sealed tube
6: 1.) cupric nitrate trihydrate; 2.) hydrogen / 2.) platinum / 1.) acetic anhydride, 10 deg C, 30 min; 2.) methanol
7: 60 percent / lithium aluminum hydride / tetrahydrofuran / 1 h / Ambient temperature
8: 44 percent / sodium cyanoborohydride / Ambient temperature; pH 5-6
9: 76 percent / boron tribromide / CH2Cl2 / 1.) -78 deg C; 2.) 10 deg C
With potassium hydroxide; sodium tetrahydroborate; sodium periodate; lithium aluminium tetrahydride; perchloric acid; hydrogen; boron tribromide; sodium cyanoborohydride; copper(II) nitrate; lithium diisopropyl amide; palladium on activated charcoal; platinum; In tetrahydrofuran; methanol; ethanol; dichloromethane; water;
DOI:10.1248/cpb.30.2641
Guidance literature:
Multi-step reaction with 8 steps
1: potassium hydroxide / ethanol / 7 h / Heating
2: 80 percent / LDA / tetrahydrofuran / 1.) -78 deg C; 2.) to room temperature
3: hydrogen, trace of perchloric acid / 10percent palladized charcoal / methanol
4: 1.) methanolic potassium hydroxide; 2.) sodium periodate; 3.) sodium borohydride
5: 82 percent / H2O / 12 h / 180 °C / in sealed tube
6: 1.) cupric nitrate trihydrate; 2.) hydrogen / 2.) platinum / 1.) acetic anhydride, 10 deg C, 30 min; 2.) methanol
7: 60 percent / lithium aluminum hydride / tetrahydrofuran / 1 h / Ambient temperature
8: 44 percent / sodium cyanoborohydride / Ambient temperature; pH 5-6
With potassium hydroxide; sodium tetrahydroborate; sodium periodate; lithium aluminium tetrahydride; perchloric acid; hydrogen; sodium cyanoborohydride; copper(II) nitrate; lithium diisopropyl amide; palladium on activated charcoal; platinum; In tetrahydrofuran; methanol; ethanol; water;
DOI:10.1248/cpb.30.2641
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