4aα-Methyl-A-homo-B,19-dinor-5β,10α-androstane-3β,17β-diol 3-Acetate 17-Cyclohexanecarboxylate

Base Information

Chemical Name:4aα-Methyl-A-homo-B,19-dinor-5β,10α-androstane-3β,17β-diol 3-Acetate 17-Cyclohexanecarboxylate
CAS No.:126792-31-2
Molecular Formula:C₂₈H₄₄O₄
Molecular Weight:444.655
Hs Code.:

Synonyms:4aα-Methyl-A-homo-B,19-dinor-5β,10α-androstane-3β,17β-diol 3-Acetate 17-Cyclohexanecarboxylate

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Chemical Property of 4aα-Methyl-A-homo-B,19-dinor-5β,10α-androstane-3β,17β-diol 3-Acetate 17-Cyclohexanecarboxylate

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Technology Process of 4aα-Methyl-A-homo-B,19-dinor-5β,10α-androstane-3β,17β-diol 3-Acetate 17-Cyclohexanecarboxylate

There total 4 articles about 4aα-Methyl-A-homo-B,19-dinor-5β,10α-androstane-3β,17β-diol 3-Acetate 17-Cyclohexanecarboxylate 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: 42.0%

: 126792-29-8
4a-Methyleno-A-homo-B,19-dinor-5β-androst-9-ene-3β,17β-diol 3-Acetate 17-Benzoate

: 126792-31-2
4aα-Methyl-A-homo-B,19-dinor-5β,10α-androstane-3β,17β-diol 3-Acetate 17-Cyclohexanecarboxylate

Guidance literature:: With hydrogen; platinum(IV) oxide; In acetic acid; for 6h; Ambient temperature;

Reference yield:

: 6961-53-1
3β-Acetoxy-6β-chloro-5-methyl-19-nor-5β-androst-9-en-17-one

: 126792-31-2
4aα-Methyl-A-homo-B,19-dinor-5β,10α-androstane-3β,17β-diol 3-Acetate 17-Cyclohexanecarboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: 93 percent / Lithium terc-butoxyaluminium hydride / tetrahydrofuran / 1 h / Ambient temperature

2: 78 percent / Pyridine / 2 h / Ambient temperature

3: 44 percent / Silver Acetate / acetic acid / 20 h / Heating

4: 42 percent / Hydrogen / Platinum oxide / acetic acid / 6 h / Ambient temperature

With pyridine; lithium tert-butoxyaluminium hydride; hydrogen; silver(I) acetate; platinum(IV) oxide; In tetrahydrofuran; acetic acid;

Reference yield:

: 126792-23-2
6β-Chloro-5-methyl-19-nor-5β-androst-9-ene-3β,17β-diol 3-Acetate

: 126792-31-2
4aα-Methyl-A-homo-B,19-dinor-5β,10α-androstane-3β,17β-diol 3-Acetate 17-Cyclohexanecarboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 78 percent / Pyridine / 2 h / Ambient temperature

2: 44 percent / Silver Acetate / acetic acid / 20 h / Heating

3: 42 percent / Hydrogen / Platinum oxide / acetic acid / 6 h / Ambient temperature

With pyridine; hydrogen; silver(I) acetate; platinum(IV) oxide; In acetic acid;