5-{3-[(2-chloro-3-trifluoromethyl-benzyl)-(2,2-diphenyl-ethyl)-amino]-propoxy}-1,2,3,4-tetrahydro-naphthalene-1-carboxylic acid

Base Information

Chemical Name:5-{3-[(2-chloro-3-trifluoromethyl-benzyl)-(2,2-diphenyl-ethyl)-amino]-propoxy}-1,2,3,4-tetrahydro-naphthalene-1-carboxylic acid
CAS No.:848171-53-9
Molecular Formula:C₃₆H₃₅ClF₃NO₃
Molecular Weight:622.127
Hs Code.:

Synonyms:5-{3-[(2-chloro-3-trifluoromethyl-benzyl)-(2,2-diphenyl-ethyl)-amino]-propoxy}-1,2,3,4-tetrahydro-naphthalene-1-carboxylic acid

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Chemical Property of 5-{3-[(2-chloro-3-trifluoromethyl-benzyl)-(2,2-diphenyl-ethyl)-amino]-propoxy}-1,2,3,4-tetrahydro-naphthalene-1-carboxylic acid

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Technology Process of 5-{3-[(2-chloro-3-trifluoromethyl-benzyl)-(2,2-diphenyl-ethyl)-amino]-propoxy}-1,2,3,4-tetrahydro-naphthalene-1-carboxylic acid

There total 8 articles about 5-{3-[(2-chloro-3-trifluoromethyl-benzyl)-(2,2-diphenyl-ethyl)-amino]-propoxy}-1,2,3,4-tetrahydro-naphthalene-1-carboxylic acid 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: 15.0%

: 848086-72-6
5-{3-[(2-chloro-3-trifluoromethyl-benzyl)-(2,2-diphenyl-ethyl)-amino]-propoxy}-1,2,3,4-tetrahydro-naphthalene-1-carboxylic acid methyl ester

: 848171-53-9
5-{3-[(2-chloro-3-trifluoromethyl-benzyl)-(2,2-diphenyl-ethyl)-amino]-propoxy}-1,2,3,4-tetrahydro-naphthalene-1-carboxylic acid

Guidance literature:: With lithium chloride; In N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2009.08.036

Reference yield:

: 93118-03-7
2-chloro-3-trifluoromethylbenzaldehyde

: 848171-53-9
5-{3-[(2-chloro-3-trifluoromethyl-benzyl)-(2,2-diphenyl-ethyl)-amino]-propoxy}-1,2,3,4-tetrahydro-naphthalene-1-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: sodium tris(acetoxy)borohydride; acetic acid / dichloromethane / 1.5 h / 20 °C

2: potassium carbonate / acetonitrile / 48 h / Heating / reflux

3: potassium carbonate; sodium iodide / acetonitrile / 16 h / Heating / reflux

4: lithium chloride / N,N-dimethyl-formamide / 5 h / Heating / reflux

With sodium tris(acetoxy)borohydride; potassium carbonate; acetic acid; sodium iodide; lithium chloride; In dichloromethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 848086-70-4
5-benzyloxy-1,2,3,4-tetrahydro-naphthalene-1-carbaldehyde

: 848171-53-9
5-{3-[(2-chloro-3-trifluoromethyl-benzyl)-(2,2-diphenyl-ethyl)-amino]-propoxy}-1,2,3,4-tetrahydro-naphthalene-1-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1: chromium(VI) oxide; sulfuric acid / water; acetone / 3 h / 0 - 20 °C

2: sulfuric acid / 2 h / Heating / reflux

3: hydrogen / palladium on activated charcoal / methanol / 16 h

4: potassium carbonate; sodium iodide / acetonitrile / 16 h / Heating / reflux

5: lithium chloride / N,N-dimethyl-formamide / 5 h / Heating / reflux

With chromium(VI) oxide; sulfuric acid; hydrogen; potassium carbonate; sodium iodide; lithium chloride; palladium on activated charcoal; In methanol; water; N,N-dimethyl-formamide; acetone; acetonitrile;