(+/-)-6,9a-methanoprostaglandin I2

Base Information

Chemical Name:(+/-)-6,9a-methanoprostaglandin I2
CAS No.:71773-69-8
Molecular Formula:C₂₁H₃₄O₄
Molecular Weight:350.499
Hs Code.:

Synonyms:

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (+/-)-6,9a-methanoprostaglandin I2

Chemical Property:

Purity/Quality:

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Technology Process of (+/-)-6,9a-methanoprostaglandin I2

There total 49 articles about (+/-)-6,9a-methanoprostaglandin I2 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:

: 5-[(3aS,4R,5R,6aS)-5-Acetoxy-4-((E)-(S)-3-acetoxy-oct-1-enyl)-hexahydro-pentalen-(2E)-ylidene]-pentanoic acid ethyl ester

: 5-[(3aR,4S,5S,6aR)-5-Hydroxy-4-((E)-(R)-1-hydroxy-oct-2-enyl)-hexahydro-pentalen-(2E)-ylidene]-pentanoic acid

: 69552-46-1,69609-77-4,69609-79-6,69609-80-9,71773-66-5,71773-67-6,71773-68-7,71773-69-8,71884-21-4,71884-22-5,74035-39-5,87828-10-2,89888-72-2,89888-73-3,89888-74-4,102491-28-1,102491-29-2,123247-51-8,138381-59-6,138381-60-9
(+/-)-6,9a-methanoprostaglandin I2

Guidance literature:: With lithium hydroxide; In methanol; at 20 ℃; for 4h;
DOI:10.1021/ja002974x

Reference yield:

: (2E,5E)-5-Allyl-deca-2,5-dienedioic acid 10-ethyl ester

: 69552-46-1,69609-77-4,69609-79-6,69609-80-9,71773-66-5,71773-67-6,71773-68-7,71773-69-8,71884-21-4,71884-22-5,74035-39-5,87828-10-2,89888-72-2,89888-73-3,89888-74-4,102491-28-1,102491-29-2,123247-51-8,138381-59-6,138381-60-9
(+/-)-6,9a-methanoprostaglandin I2

Guidance literature:: Multi-step reaction with 6 steps

1.1: 67 percent / DMAP; DCC / CH₂Cl₂ / 2 h / 20 °C

2.1: ClTi(O-i-Pr)3; i-PrMgCl / diethyl ether; hexane / 6 h / -40 °C

2.2: diethyl ether; hexane / 0.5 h / -50 - -20 °C

3.1: 55 mg / NaBH₄ / methanol / 1 h / 0 °C

4.1: 97 percent / pyridine / 24 h / 20 °C

5.1: PdCl₂(CH₃CN)2 / tetrahydrofuran / 3 h / 20 °C

6.1: 46 mg / LiOH / methanol / 4 h / 20 °C

With pyridine; triisopropoxytitanium(IV) chloride; dmap; dichloro bis(acetonitrile) palladium(II); lithium hydroxide; sodium tetrahydroborate; isopropylmagnesium chloride; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane;
DOI:10.1021/ja002974x

Reference yield:

: 2548-87-0
(E)-2-Octenal

: 69552-46-1,69609-77-4,69609-79-6,69609-80-9,71773-66-5,71773-67-6,71773-68-7,71773-69-8,71884-21-4,71884-22-5,74035-39-5,87828-10-2,89888-72-2,89888-73-3,89888-74-4,102491-28-1,102491-29-2,123247-51-8,138381-59-6,138381-60-9
(+/-)-6,9a-methanoprostaglandin I2

Guidance literature:: Multi-step reaction with 5 steps

1.1: ClTi(O-i-Pr)3; i-PrMgCl / diethyl ether; hexane / 6 h / -40 °C

1.2: diethyl ether; hexane / 0.5 h / -50 - -20 °C

2.1: 55 mg / NaBH₄ / methanol / 1 h / 0 °C

3.1: 97 percent / pyridine / 24 h / 20 °C

4.1: PdCl₂(CH₃CN)2 / tetrahydrofuran / 3 h / 20 °C

5.1: 46 mg / LiOH / methanol / 4 h / 20 °C

With pyridine; triisopropoxytitanium(IV) chloride; dichloro bis(acetonitrile) palladium(II); lithium hydroxide; sodium tetrahydroborate; isopropylmagnesium chloride; In tetrahydrofuran; methanol; diethyl ether; hexane;
DOI:10.1021/ja002974x