Benzoic acid (1S,12bS)-1-ethyl-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizin-1-ylmethyl ester

Base Information

Chemical Name:Benzoic acid (1S,12bS)-1-ethyl-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizin-1-ylmethyl ester
CAS No.:97805-31-7
Molecular Formula:C₂₅H₂₈N₂O₂
Molecular Weight:388.51
Hs Code.:

Synonyms:Benzoic acid (1S,12bS)-1-ethyl-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizin-1-ylmethyl ester

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Chemical Property of Benzoic acid (1S,12bS)-1-ethyl-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizin-1-ylmethyl ester

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Technology Process of Benzoic acid (1S,12bS)-1-ethyl-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizin-1-ylmethyl ester

There total 2 articles about Benzoic acid (1S,12bS)-1-ethyl-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizin-1-ylmethyl ester 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: 95.9%

: 64361-56-4
1α-ethyl-1β-(hydroxymethyl)-1,2,3,4,6,7,12,12bβ-octahydroindolo<2,3-a>quinolizine

: 98-88-4
benzoyl chloride

: 97805-31-7
Benzoic acid (1S,12bS)-1-ethyl-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizin-1-ylmethyl ester

Guidance literature:: With pyridine; for 1h; Ambient temperature;
DOI:10.1021/jo00220a017

Reference yield:

: 55390-29-9
1-ethyl-2,3,4,6,7,12-hexahydro-indolo(2,3-a)quinolizinium perchlorate

: 97805-31-7
Benzoic acid (1S,12bS)-1-ethyl-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizin-1-ylmethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) 2M NaOH / 1.) CH₂Cl₂, H₂O, 10 min, 2.) 160-170 deg C, 4h

2: 95.9 percent / pyridine / 1 h / Ambient temperature

With pyridine; sodium hydroxide;
DOI:10.1021/jo00220a017