(1aR,3aR,3bS,5aR,6R,8aS,8bS,10aR)-10-Benzyloxy-6-((R)-4-ethyl-1,5-dimethyl-hexyl)-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalene

Base Information

Chemical Name:(1aR,3aR,3bS,5aR,6R,8aS,8bS,10aR)-10-Benzyloxy-6-((R)-4-ethyl-1,5-dimethyl-hexyl)-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalene
CAS No.:126474-60-0
Molecular Formula:C₃₆H₅₆O
Molecular Weight:504.84
Hs Code.:

(1aR,3aR,3bS,5aR,6R,8aS,8bS,10aR)-10-Benzyloxy-6-((R)-4-ethyl-1,5-dimethyl-hexyl)-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalene

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Chemical Property of (1aR,3aR,3bS,5aR,6R,8aS,8bS,10aR)-10-Benzyloxy-6-((R)-4-ethyl-1,5-dimethyl-hexyl)-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalene

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Technology Process of (1aR,3aR,3bS,5aR,6R,8aS,8bS,10aR)-10-Benzyloxy-6-((R)-4-ethyl-1,5-dimethyl-hexyl)-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalene

There total 1 articles about (1aR,3aR,3bS,5aR,6R,8aS,8bS,10aR)-10-Benzyloxy-6-((R)-4-ethyl-1,5-dimethyl-hexyl)-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalene 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:

: 124-63-0
methanesulfonyl chloride

: 126474-57-5
Methanesulfonic acid (3S,8S,9S,10R,13R,14S,17R)-17-((R)-4-ethyl-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester

: 126474-64-4
(3R,8S,9S,10R,13R,14S,17R)-3-Benzyloxy-17-((R)-4-ethyl-1,5-dimethyl-hexyl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene

: 126474-60-0
(1aR,3aR,3bS,5aR,6R,8aS,8bS,10aR)-10-Benzyloxy-6-((R)-4-ethyl-1,5-dimethyl-hexyl)-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalene

Guidance literature:: With pyridine; In dichloromethane; for 4h;

Reference yield:

: 126474-60-0
(1aR,3aR,3bS,5aR,6R,8aS,8bS,10aR)-10-Benzyloxy-6-((R)-4-ethyl-1,5-dimethyl-hexyl)-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalene

: 106560-66-1
(20S)-6β-benzyloxy-3α,5-cyclo-5α-pregnane-20-carboxaldehyde

: 126474-65-5
Benzoic acid (1aR,3aR,3bS,5aR,6R,8aS,8bS,10aR)-6-((R)-4-ethyl-1,5-dimethyl-hexyl)-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalen-10-yl ester

Guidance literature:: With dimethylsulfide; 6β-benzyloxy-3α,5-cyclosteroids; sodium carbonate; ozone; Yield given. Multistep reaction; 1.) CH₂Cl₂, -78 deg C, 2.) -78 deg C, 10 min; 0 deg C, 8 h;