(3aR,10aS)-5-Benzyl-3a-(2-methyl-allyl)-decahydro-10-oxa-5-aza-cyclopenta[d]naphthalen-6-one

Base Information

• Chemical Name: (3aR,10aS)-5-Benzyl-3a-(2-methyl-allyl)-decahydro-10-oxa-5-aza-cyclopenta[d]naphthalen-6-one
• CAS No.: 111794-94-6
• Molecular Formula: C₂₂H₂₉NO₂
• Molecular Weight: 339.478
• Mol file: 111794-94-6.mol

Synonyms:(3aR,10aS)-5-Benzyl-3a-(2-methyl-allyl)-decahydro-10-oxa-5-aza-cyclopenta[d]naphthalen-6-one

Chemical Property of (3aR,10aS)-5-Benzyl-3a-(2-methyl-allyl)-decahydro-10-oxa-5-aza-cyclopenta[d]naphthalen-6-one

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (3aR,10aS)-5-Benzyl-3a-(2-methyl-allyl)-decahydro-10-oxa-5-aza-cyclopenta[d]naphthalen-6-one

There total 7 articles about (3aR,10aS)-5-Benzyl-3a-(2-methyl-allyl)-decahydro-10-oxa-5-aza-cyclopenta[d]naphthalen-6-one 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: 90.0%

(4aR,7aS)-2-Benzyl-4-(3-bromo-propyl)-4a-hydroxy-7a-(2-methyl-allyl)-octahydro-[2]pyrindin-3-one (111795-00-7) → (3aR,10aS)-5-Benzyl-3a-(2-methyl-allyl)-decahydro-10-oxa-5-aza-cyclopenta[d]naphthalen-6-one (111794-94-6)

Guidance literature:

With potassium tert-butylate; In tert-butyl alcohol;

DOI:10.1021/jo00235a020

Reference yield: 73.0%

2,5-Dibromo-pentanoic acid benzyl-[1-(2-methyl-allyl)-2-oxo-cyclopentylmethyl]-amide (111794-93-5,111794-95-7) → (3aR,10aS)-5-Benzyl-3a-(2-methyl-allyl)-decahydro-10-oxa-5-aza-cyclopenta[d]naphthalen-6-one (111794-94-6)

Guidance literature:

With tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; 1.) THF, 0 deg C, 2.) THF, RT;

DOI:10.1021/jo00235a020

Reference yield:

2,5-Dibromopentanoic Acid Bromide (89180-84-7) → (3aR,10aS)-5-Benzyl-3a-(2-methyl-allyl)-decahydro-10-oxa-5-aza-cyclopenta[d]naphthalen-6-one (111794-94-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 90 percent

2: 73 percent / 1.) THF, 2.) HMPA / 1.) THF, 0 deg C, 2.) THF, RT

With tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide;

DOI:10.1021/jo00235a020

upstream raw materials:

(4aR,7aS)-2-Benzyl-4-(3-bromo-propyl)-4a-hydroxy-7a-(2-methyl-allyl)-octahydro-[2]pyrindin-3-one

2,5-Dibromo-pentanoic acid benzyl-[1-(2-methyl-allyl)-2-oxo-cyclopentylmethyl]-amide

2,5-Dibromopentanoic Acid Bromide

ethyl 2-ethoxycyclopent-1-ene-carboxylate