(3aS,6aR,11bR)-3-(3-Allyloxy-propyl)-7-benzyl-3a-hydroxy-3a,4,5,6,6a,7-hexahydro-3H-pyrrolo[2,3-d]carbazol-2-one

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Chemical Name:(3aS,6aR,11bR)-3-(3-Allyloxy-propyl)-7-benzyl-3a-hydroxy-3a,4,5,6,6a,7-hexahydro-3H-pyrrolo[2,3-d]carbazol-2-one
CAS No.:142288-04-8
Molecular Formula:C₂₇H₃₂N₂O₃
Molecular Weight:432.563
Hs Code.:

Synonyms:(3aS,6aR,11bR)-3-(3-Allyloxy-propyl)-7-benzyl-3a-hydroxy-3a,4,5,6,6a,7-hexahydro-3H-pyrrolo[2,3-d]carbazol-2-one

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Chemical Property of (3aS,6aR,11bR)-3-(3-Allyloxy-propyl)-7-benzyl-3a-hydroxy-3a,4,5,6,6a,7-hexahydro-3H-pyrrolo[2,3-d]carbazol-2-one

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Technology Process of (3aS,6aR,11bR)-3-(3-Allyloxy-propyl)-7-benzyl-3a-hydroxy-3a,4,5,6,6a,7-hexahydro-3H-pyrrolo[2,3-d]carbazol-2-one

There total 4 articles about (3aS,6aR,11bR)-3-(3-Allyloxy-propyl)-7-benzyl-3a-hydroxy-3a,4,5,6,6a,7-hexahydro-3H-pyrrolo[2,3-d]carbazol-2-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:

: 105939-61-5
3-(allyloxy)propan-1-amine

: 142288-04-8
(3aS,6aR,11bR)-3-(3-Allyloxy-propyl)-7-benzyl-3a-hydroxy-3a,4,5,6,6a,7-hexahydro-3H-pyrrolo[2,3-d]carbazol-2-one

Guidance literature:: Multi-step reaction with 3 steps

1: NEt₃ / diethyl ether / 1 h / 0 °C

2: 100 percent / NaI / acetone / 12 h / Heating

3: 1.) KH / 1.) THF, RT, 5 min, 2.) THF, 10 min

With potassium hydride; triethylamine; sodium iodide; In diethyl ether; acetone;
DOI:10.1080/00397919208021293

Reference yield:

: 142288-03-7
3-(3-Azido-propoxy)-propene

: 142288-04-8
(3aS,6aR,11bR)-3-(3-Allyloxy-propyl)-7-benzyl-3a-hydroxy-3a,4,5,6,6a,7-hexahydro-3H-pyrrolo[2,3-d]carbazol-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: LiAlH₄ / diethyl ether / 10 h

2: NEt₃ / diethyl ether / 1 h / 0 °C

3: 100 percent / NaI / acetone / 12 h / Heating

4: 1.) KH / 1.) THF, RT, 5 min, 2.) THF, 10 min

With lithium aluminium tetrahydride; potassium hydride; triethylamine; sodium iodide; In diethyl ether; acetone;
DOI:10.1080/00397919208021293

Reference yield:

: 13219-22-2
N-(3-allyloxypropyl)chloroacetamide

: 142288-04-8
(3aS,6aR,11bR)-3-(3-Allyloxy-propyl)-7-benzyl-3a-hydroxy-3a,4,5,6,6a,7-hexahydro-3H-pyrrolo[2,3-d]carbazol-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / NaI / acetone / 12 h / Heating

2: 1.) KH / 1.) THF, RT, 5 min, 2.) THF, 10 min

With potassium hydride; sodium iodide; In acetone;
DOI:10.1080/00397919208021293