(17Z)-{1-[4-(methyloxycarbonyl)phenyl]methylidene}-de-A,B-androstan-8β-ol

Base Information

Chemical Name:(17Z)-{1-[4-(methyloxycarbonyl)phenyl]methylidene}-de-A,B-androstan-8β-ol
CAS No.:282724-90-7
Molecular Formula:C₁₉H₂₄O₃
Molecular Weight:300.398
Hs Code.:

Synonyms:(17Z)-{1-[4-(methyloxycarbonyl)phenyl]methylidene}-de-A,B-androstan-8β-ol

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Chemical Property of (17Z)-{1-[4-(methyloxycarbonyl)phenyl]methylidene}-de-A,B-androstan-8β-ol

Chemical Property:

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Technology Process of (17Z)-{1-[4-(methyloxycarbonyl)phenyl]methylidene}-de-A,B-androstan-8β-ol

There total 5 articles about (17Z)-{1-[4-(methyloxycarbonyl)phenyl]methylidene}-de-A,B-androstan-8β-ol 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: 92.0%

: 307318-58-7
8β-tert-butyldimethylsilyloxy-(17Z)-{1-[4-(methyloxycarbonyl)phenyl]methylidene}-de-A,B-androstane

: 282724-90-7
(17Z)-{1-[4-(methyloxycarbonyl)phenyl]methylidene}-de-A,B-androstan-8β-ol

Guidance literature:: With hydrogen fluoride; In acetonitrile; at 20 ℃; for 3h;
DOI:10.1021/jo000579j

Reference yield:

: 38186-51-5
diethyl (4-bromobenzyl)phosphonate

: 282724-90-7
(17Z)-{1-[4-(methyloxycarbonyl)phenyl]methylidene}-de-A,B-androstan-8β-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 13 percent / KH / tetrahydrofuran / 4 h / Heating

2: 80 percent / Et₃N; dppp / Pd(OAc)2 / dimethylsulfoxide / 12 h / 80 °C

3: 75 percent / tetrahydrofuran / 1.5 h / Irradiation

4: 92 percent / aq. HF / acetonitrile / 3 h / 20 °C

With 1,3-bis-(diphenylphosphino)propane; hydrogen fluoride; potassium hydride; triethylamine; palladium diacetate; In tetrahydrofuran; dimethyl sulfoxide; acetonitrile; 1: Condensation / 2: Addition / 3: Isomerization / 4: Decomposition;
DOI:10.1021/jo000579j

Reference yield:

: 140659-26-3
8β-[(tert-butyldimethylsilyl)oxy]de-A,B-androstan-17β-one

: 282724-90-7
(17Z)-{1-[4-(methyloxycarbonyl)phenyl]methylidene}-de-A,B-androstan-8β-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 13 percent / KH / tetrahydrofuran / 4 h / Heating

2: 80 percent / Et₃N; dppp / Pd(OAc)2 / dimethylsulfoxide / 12 h / 80 °C

3: 75 percent / tetrahydrofuran / 1.5 h / Irradiation

4: 92 percent / aq. HF / acetonitrile / 3 h / 20 °C

With 1,3-bis-(diphenylphosphino)propane; hydrogen fluoride; potassium hydride; triethylamine; palladium diacetate; In tetrahydrofuran; dimethyl sulfoxide; acetonitrile; 1: Condensation / 2: Addition / 3: Isomerization / 4: Decomposition;
DOI:10.1021/jo000579j