5-Benzoyl-6α-benzoxy-7,7,9-trimethyl-5,6α,6aβ,7,8,10aβ-hexahydroindeno-<2,1-b>indole

Base Information

Chemical Name:5-Benzoyl-6α-benzoxy-7,7,9-trimethyl-5,6α,6aβ,7,8,10aβ-hexahydroindeno-<2,1-b>indole
CAS No.:135630-37-4
Molecular Formula:C₃₂H₂₉NO₃
Molecular Weight:475.587
Hs Code.:

Synonyms:5-Benzoyl-6α-benzoxy-7,7,9-trimethyl-5,6α,6aβ,7,8,10aβ-hexahydroindeno-<2,1-b>indole

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Chemical Property of 5-Benzoyl-6α-benzoxy-7,7,9-trimethyl-5,6α,6aβ,7,8,10aβ-hexahydroindeno-<2,1-b>indole

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Technology Process of 5-Benzoyl-6α-benzoxy-7,7,9-trimethyl-5,6α,6aβ,7,8,10aβ-hexahydroindeno-<2,1-b>indole

There total 9 articles about 5-Benzoyl-6α-benzoxy-7,7,9-trimethyl-5,6α,6aβ,7,8,10aβ-hexahydroindeno-<2,1-b>indole 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: 76.0%

: 120094-32-8,124600-45-9,135683-71-5,143615-53-6
6α-Hydroxy-7,7,9-trimethyl-5,6α,6aβ,7,8,10aβ-hexahydroindeno-<2,1-b>indole

: 98-88-4
benzoyl chloride

: 135630-37-4
5-Benzoyl-6α-benzoxy-7,7,9-trimethyl-5,6α,6aβ,7,8,10aβ-hexahydroindeno-<2,1-b>indole

Guidance literature:: With dmap; triethylamine; In dichloromethane; 1) RT, 2) reflux, 1 d;
DOI:10.1139/v91-141

Reference yield:

: 124549-81-1
2β-Benzoxy-4,6,6-trimethylcyclohex-3-ene-1β-carboxylic benzoic anhydride

: 135630-37-4
5-Benzoyl-6α-benzoxy-7,7,9-trimethyl-5,6α,6aβ,7,8,10aβ-hexahydroindeno-<2,1-b>indole

Guidance literature:: Multi-step reaction with 6 steps

1: 40 percent / diethyl ether; CH₂Cl₂ / 5 °C

2: benzene

3: diethyl ether; CH₂Cl₂ / -15 °C

4: MeONa / methanol / Heating

5: 65 percent / LiAlH₄ / tetrahydrofuran

6: DMAP, Et₃N / CH₂Cl₂ / Heating

With dmap; lithium aluminium tetrahydride; sodium methylate; triethylamine; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; benzene;

Reference yield:

: 120094-31-7,124549-86-6,133054-04-3
6-Oxo-7,7-9-trimethyl-5,6,6aα,7,8,10αβ-hexahydroindeno-<2,1-b>indole

: 135630-37-4
5-Benzoyl-6α-benzoxy-7,7,9-trimethyl-5,6α,6aβ,7,8,10aβ-hexahydroindeno-<2,1-b>indole

Guidance literature:: Multi-step reaction with 3 steps

1: MeONa / methanol / Heating

2: 65 percent / LiAlH₄ / tetrahydrofuran

3: DMAP, Et₃N / CH₂Cl₂ / Heating

With dmap; lithium aluminium tetrahydride; sodium methylate; triethylamine; In tetrahydrofuran; methanol; dichloromethane;