(3R,6R)-6-methyl-3-phenyl-2,3,6,10b-tetrahydro-5H-oxazolo[2,3-a]isoquinoline

Base Information

• Chemical Name: (3R,6R)-6-methyl-3-phenyl-2,3,6,10b-tetrahydro-5H-oxazolo[2,3-a]isoquinoline
• CAS No.: 503822-39-7
• Molecular Formula: C₁₈H₁₉NO
• Molecular Weight: 265.355
• Mol file: 503822-39-7.mol

Synonyms:(3R,6R)-6-methyl-3-phenyl-2,3,6,10b-tetrahydro-5H-oxazolo[2,3-a]isoquinoline

Chemical Property of (3R,6R)-6-methyl-3-phenyl-2,3,6,10b-tetrahydro-5H-oxazolo[2,3-a]isoquinoline

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (3R,6R)-6-methyl-3-phenyl-2,3,6,10b-tetrahydro-5H-oxazolo[2,3-a]isoquinoline

There total 3 articles about (3R,6R)-6-methyl-3-phenyl-2,3,6,10b-tetrahydro-5H-oxazolo[2,3-a]isoquinoline 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:

D-2-phenylglycinol (56613-80-0) → (3R,6R)-6-methyl-3-phenyl-2,3,6,10b-tetrahydro-5H-oxazolo[2,3-a]isoquinoline (503822-39-7)

Guidance literature:

Multi-step reaction with 3 steps

1: 75 percent / K₂CO₃ / tetrahydrofuran / 16 h / 20 °C

2: benzene / 2 h / Heating

3: Bu₃SnH; AIBN / benzene / 1 h / Heating

With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; potassium carbonate; In tetrahydrofuran; benzene;

DOI:10.3987/com-02-s(m)42

Reference yield:

(R)-2-(allylamino)-2-phenylethanol (503822-33-1) → (3R,6R)-6-methyl-3-phenyl-2,3,6,10b-tetrahydro-5H-oxazolo[2,3-a]isoquinoline (503822-39-7)

Guidance literature:

Multi-step reaction with 2 steps

1: benzene / 2 h / Heating

2: Bu₃SnH; AIBN / benzene / 1 h / Heating

With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In benzene;

DOI:10.3987/com-02-s(m)42

Reference yield:

(2R,4R)-3-allyl-2-(2-bromophenyl)-4-phenyl-1,3-oxazolidine (503822-36-4) → (3R,6R)-6-methyl-3-phenyl-2,3,6,10b-tetrahydro-5H-oxazolo[2,3-a]isoquinoline (503822-39-7) + (3R,6S)-6-methyl-3-phenyl-2,3,6,10b-tetrahydro-5H-oxazolo[2,3-a]isoquinoline + (3R)-3-phenyl-2,3,4,5,6,10b-hexahydro-1-oxo-3a-azabenzo[e]azulene (503822-42-2)

Guidance literature:

With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In benzene; for 1h; Heating;

DOI:10.3987/com-02-s(m)42

upstream raw materials:

(2R,4R)-3-allyl-2-(2-bromophenyl)-4-phenyl-1,3-oxazolidine

D-2-phenylglycinol

(R)-2-(allylamino)-2-phenylethanol

Downstream raw materials:

(R)-4-methyl-1,2,3,4-tetrahydroisoquinoline

(1'R,4S)-2-(2'-hydroxy-1'-phenylethyl)-4-methyl-1,2,3,4-tetrahydroisoquinoline