(1R,2R)-2-(1-phenethyl-3-phenyl-prop-2-ynylamino)-2-phenyl-ethanol

Base Information

• Chemical Name: (1R,2R)-2-(1-phenethyl-3-phenyl-prop-2-ynylamino)-2-phenyl-ethanol
• CAS No.: 306747-36-4
• Molecular Formula: C₂₅H₂₅NO
• Molecular Weight: 355.48
• Mol file: 306747-36-4.mol

Synonyms:(1R,2R)-2-(1-phenethyl-3-phenyl-prop-2-ynylamino)-2-phenyl-ethanol

Chemical Property of (1R,2R)-2-(1-phenethyl-3-phenyl-prop-2-ynylamino)-2-phenyl-ethanol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (1R,2R)-2-(1-phenethyl-3-phenyl-prop-2-ynylamino)-2-phenyl-ethanol

There total 1 articles about (1R,2R)-2-(1-phenethyl-3-phenyl-prop-2-ynylamino)-2-phenyl-ethanol 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:

Reference yield: 87.0%

3-phenyl-propionaldehyde (104-53-0) + D-2-phenylglycinol (56613-80-0) + phenylacetylene (536-74-3) → (1R,2R)-2-(1-phenethyl-3-phenyl-prop-2-ynylamino)-2-phenyl-ethanol (306747-36-4)

Guidance literature:

Multistep reaction.;

DOI:10.1021/jo0003706

Reference yield: 51.0%

(1R,2R)-2-(1-phenethyl-3-phenyl-prop-2-ynylamino)-2-phenyl-ethanol (306747-36-4) → (1R)-phenethyl-3-phenyl-prop-2-ynylamine (306747-42-2)

Guidance literature:

(1R,2R)-2-(1-phenethyl-3-phenyl-prop-2-ynylamino)-2-phenyl-ethanol; With periodic acid; methylamine; In methanol; at 20 ℃; for 3h;

With hydrogenchloride; In methanol; Further stages.;

DOI:10.1021/jo0003706

Reference yield:

(1R,2R)-2-(1-phenethyl-3-phenyl-prop-2-ynylamino)-2-phenyl-ethanol (306747-36-4) → (1R)-N-(1-phenethyl-3-phenyl-prop-2-ynyl)-benzamide

Guidance literature:

Multi-step reaction with 2 steps

1.1: aq. H₅IO₆; aq. MeNH₂ / methanol / 3 h / 20 °C

1.2: 51 percent / aq. HCl / methanol

2.1: 61 percent / Et₃N / CH₂Cl₂

With periodic acid; triethylamine; methylamine; In methanol; dichloromethane; 1.1: Oxidation / 1.2: Hydrolysis / 2.1: Acylation;

DOI:10.1021/jo0003706

upstream raw materials:

3-phenyl-propionaldehyde

D-2-phenylglycinol

phenylacetylene

Downstream raw materials:

(1R)-phenethyl-3-phenyl-prop-2-ynylamine