tert-butyl 2-(7-(4-(cyclopropylmethoxy)-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1Hpyrrolo[1,2-a]indol-1-yl)acetate

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Chemical Name:tert-butyl 2-(7-(4-(cyclopropylmethoxy)-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1Hpyrrolo[1,2-a]indol-1-yl)acetate
CAS No.:1215118-85-6
Molecular Formula:C₂₉H₃₂F₃NO₄
Molecular Weight:515.573
Hs Code.:

Synonyms:tert-butyl 2-(7-(4-(cyclopropylmethoxy)-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1Hpyrrolo[1,2-a]indol-1-yl)acetate

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Chemical Property of tert-butyl 2-(7-(4-(cyclopropylmethoxy)-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1Hpyrrolo[1,2-a]indol-1-yl)acetate

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Technology Process of tert-butyl 2-(7-(4-(cyclopropylmethoxy)-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1Hpyrrolo[1,2-a]indol-1-yl)acetate

There total 7 articles about tert-butyl 2-(7-(4-(cyclopropylmethoxy)-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1Hpyrrolo[1,2-a]indol-1-yl)acetate 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:

: 1206124-87-9
4-(chloromethyl)-1-(cyclopropylmethoxy)-2-(trifluoromethyl)benzene

: 1215118-65-2
tert-butyl 2-(7-hydroxy-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetate

: 1215118-85-6
tert-butyl 2-(7-(4-(cyclopropylmethoxy)-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1Hpyrrolo[1,2-a]indol-1-yl)acetate

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 60 ℃; for 16h;
DOI:10.1021/ml500422m

Reference yield:

: 1215119-77-9
tert-butyl 2-(7-hydroxy-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-ylidene)acetate

: 1215118-85-6
tert-butyl 2-(7-(4-(cyclopropylmethoxy)-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1Hpyrrolo[1,2-a]indol-1-yl)acetate

Guidance literature:: Multi-step reaction with 2 steps

1: palladium 10% on activated carbon; hydrogen / water; ethyl acetate / 3 h / 4913.04 Torr

2: potassium carbonate / N,N-dimethyl-formamide / 16 h / 60 °C

With palladium 10% on activated carbon; hydrogen; potassium carbonate; In water; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1021/ml500422m

Reference yield:

: 1174512-53-8
7-bromo-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-one

: 1215118-85-6
tert-butyl 2-(7-(4-(cyclopropylmethoxy)-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1Hpyrrolo[1,2-a]indol-1-yl)acetate

Guidance literature:: Multi-step reaction with 5 steps

1: tetrahydrofuran / 16 h / 65 °C

2: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate / 1,4-dioxane / 1.5 h / 90 °C / Inert atmosphere

3: sodium hydroxide; dihydrogen peroxide / tetrahydrofuran; water / 0.42 h / 23 °C

4: palladium 10% on activated carbon; hydrogen / water; ethyl acetate / 3 h / 4913.04 Torr

5: potassium carbonate / N,N-dimethyl-formamide / 16 h / 60 °C

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; palladium 10% on activated carbon; hydrogen; dihydrogen peroxide; potassium acetate; potassium carbonate; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; water; ethyl acetate; N,N-dimethyl-formamide; 1: |Wittig Olefination;
DOI:10.1021/ml500422m