4-(2,2’,6’-trimethyl-biphenyl-3-ylmethoxy)-1,1a,6,6a-tetrahydro-3-azacyclopropa[a]indene-1-carboxylic acid

Base Information

Chemical Name:4-(2,2’,6’-trimethyl-biphenyl-3-ylmethoxy)-1,1a,6,6a-tetrahydro-3-azacyclopropa[a]indene-1-carboxylic acid
CAS No.:1544741-34-5
Molecular Formula:C₂₆H₂₅NO₃
Molecular Weight:399.489
Hs Code.:

Synonyms:4-(2,2’,6’-trimethyl-biphenyl-3-ylmethoxy)-1,1a,6,6a-tetrahydro-3-azacyclopropa[a]indene-1-carboxylic acid

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Chemical Property of 4-(2,2’,6’-trimethyl-biphenyl-3-ylmethoxy)-1,1a,6,6a-tetrahydro-3-azacyclopropa[a]indene-1-carboxylic acid

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Technology Process of 4-(2,2’,6’-trimethyl-biphenyl-3-ylmethoxy)-1,1a,6,6a-tetrahydro-3-azacyclopropa[a]indene-1-carboxylic acid

There total 13 articles about 4-(2,2’,6’-trimethyl-biphenyl-3-ylmethoxy)-1,1a,6,6a-tetrahydro-3-azacyclopropa[a]indene-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:

: 1544740-94-4
4-(2,2’,6’-trimethyl-biphenyl-3-ylmethoxy)-1,1a,6,6a-tetrahydro-3-aza-cyclopropa[a]indene-1-carboxylic acid ethyl ester

: 1544741-34-5
4-(2,2’,6’-trimethyl-biphenyl-3-ylmethoxy)-1,1a,6,6a-tetrahydro-3-azacyclopropa[a]indene-1-carboxylic acid

Guidance literature:: With water; lithium hydroxide; In tetrahydrofuran; methanol; at 20 ℃; for 2h;

Reference yield:

: 1544739-11-8
(4-allyl-5-vinyl-pyridin-2-yl)-bis-(4-methoxy-benzyl)-amine

: 1544741-34-5
4-(2,2’,6’-trimethyl-biphenyl-3-ylmethoxy)-1,1a,6,6a-tetrahydro-3-azacyclopropa[a]indene-1-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride / dichloromethane / 3 h / Reflux; Inert atmosphere

2.1: rhodium(II) acetate / dichloromethane / 0.25 h

2.2: 3 h / Reflux

3.1: trifluoroacetic acid / dichloromethane / 20 °C

4.1: sulfuric acid; sodium nitrite / 2 h / 0 - 20 °C

5.1: silver carbonate / toluene / 12 h / 100 °C

6.1: water; lithium hydroxide / tetrahydrofuran; methanol / 2 h / 20 °C

With rhodium(II) acetate; tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; sulfuric acid; water; silver carbonate; trifluoroacetic acid; lithium hydroxide; sodium nitrite; In tetrahydrofuran; methanol; dichloromethane; toluene;

Reference yield:

: 1544739-13-0
4-[bis-(4-methoxy-benzyl)-amino]-1,1a,6,6a-tetrahydro-3-aza-cyclopropa[a]-indene-1-carboxylic acid ethyl ester

: 1544741-34-5
4-(2,2’,6’-trimethyl-biphenyl-3-ylmethoxy)-1,1a,6,6a-tetrahydro-3-azacyclopropa[a]indene-1-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1: trifluoroacetic acid / dichloromethane / 20 °C

2: sulfuric acid; sodium nitrite / 2 h / 0 - 20 °C

3: silver carbonate / toluene / 12 h / 100 °C

4: water; lithium hydroxide / tetrahydrofuran; methanol / 2 h / 20 °C

With sulfuric acid; water; silver carbonate; trifluoroacetic acid; lithium hydroxide; sodium nitrite; In tetrahydrofuran; methanol; dichloromethane; toluene;