3-Benzyloxycarbonyl-5-(3-benzyloxypropyl)-1,2,4,5,6,7,8,9-octahydro-3H-azecino<5,4-b>indol-8-ol

Base Information

Chemical Name:3-Benzyloxycarbonyl-5-(3-benzyloxypropyl)-1,2,4,5,6,7,8,9-octahydro-3H-azecino<5,4-b>indol-8-ol
CAS No.:107704-36-9
Molecular Formula:C₃₃H₃₈N₂O₄
Molecular Weight:526.676
Hs Code.:

Synonyms:3-Benzyloxycarbonyl-5-(3-benzyloxypropyl)-1,2,4,5,6,7,8,9-octahydro-3H-azecino<5,4-b>indol-8-ol

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Chemical Property of 3-Benzyloxycarbonyl-5-(3-benzyloxypropyl)-1,2,4,5,6,7,8,9-octahydro-3H-azecino<5,4-b>indol-8-ol

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Technology Process of 3-Benzyloxycarbonyl-5-(3-benzyloxypropyl)-1,2,4,5,6,7,8,9-octahydro-3H-azecino<5,4-b>indol-8-ol

There total 7 articles about 3-Benzyloxycarbonyl-5-(3-benzyloxypropyl)-1,2,4,5,6,7,8,9-octahydro-3H-azecino<5,4-b>indol-8-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: 70.0%

: 107688-36-8
3-(3-Benzyloxypropyl)-1,2,3,4,6,7,12,12b-octahydroindolo<2,3-a>quinolizin

: 501-53-1,94274-21-2
benzyl chloroformate

: 107704-36-9
3-Benzyloxycarbonyl-5-(3-benzyloxypropyl)-1,2,4,5,6,7,8,9-octahydro-3H-azecino<5,4-b>indol-8-ol

Guidance literature:: With potassium carbonate; In tetrahydrofuran; for 3h; Heating;
DOI:10.1016/S0040-4020(01)86686-2

Reference yield:

: 61-54-1
tryptamine

: 107704-36-9
3-Benzyloxycarbonyl-5-(3-benzyloxypropyl)-1,2,4,5,6,7,8,9-octahydro-3H-azecino<5,4-b>indol-8-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 97 percent / glacial acetic acid / 7 h / Heating

2: 1) aq. NaOH / 1) ethanol, 30 min, reflux, 2) 180 deg C, vacuum

3: 95 percent / LiAlH₄ / tetrahydrofuran / 1.5 h / Heating

4: 70 percent / 15 percent K₂CO₃ / tetrahydrofuran / 3 h / Heating

With sodium hydroxide; lithium aluminium tetrahydride; potassium carbonate; acetic acid; In tetrahydrofuran;
DOI:10.1016/S0040-4020(01)86686-2

Reference yield:

: 82258-55-7
Ethyl 5-benzyloxy-2-(ethoxycarbonyl)pentanoate

: 107704-36-9
3-Benzyloxycarbonyl-5-(3-benzyloxypropyl)-1,2,4,5,6,7,8,9-octahydro-3H-azecino<5,4-b>indol-8-ol

Guidance literature:: Multi-step reaction with 5 steps

1: 1) Na / 1) ethanol, 5 deg C, 2) 1.5 h, r.t.

2: 97 percent / glacial acetic acid / 7 h / Heating

3: 1) aq. NaOH / 1) ethanol, 30 min, reflux, 2) 180 deg C, vacuum

4: 95 percent / LiAlH₄ / tetrahydrofuran / 1.5 h / Heating

5: 70 percent / 15 percent K₂CO₃ / tetrahydrofuran / 3 h / Heating

With sodium hydroxide; lithium aluminium tetrahydride; sodium; potassium carbonate; acetic acid; In tetrahydrofuran;
DOI:10.1016/S0040-4020(01)86686-2