5-methyl-4-phenyl-1,9,9a,10a-tetrahydro-4H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene-2-carboxylic acid ethyl ester

Base Information

Chemical Name:5-methyl-4-phenyl-1,9,9a,10a-tetrahydro-4H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene-2-carboxylic acid ethyl ester
CAS No.:461641-11-2
Molecular Formula:C₂₄H₂₅NO₃
Molecular Weight:375.467
Hs Code.:

5-methyl-4-phenyl-1,9,9a,10a-tetrahydro-4<i>H</i>,4b<i>H</i>-10-oxa-4a-aza-indeno[1,2-<i>a</i>]indene-2-carboxylic acid ethyl ester

Synonyms:5-methyl-4-phenyl-1,9,9a,10a-tetrahydro-4H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene-2-carboxylic acid ethyl ester

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Chemical Property of 5-methyl-4-phenyl-1,9,9a,10a-tetrahydro-4H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene-2-carboxylic acid ethyl ester

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Technology Process of 5-methyl-4-phenyl-1,9,9a,10a-tetrahydro-4H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene-2-carboxylic acid ethyl ester

There total 8 articles about 5-methyl-4-phenyl-1,9,9a,10a-tetrahydro-4H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene-2-carboxylic acid ethyl 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:

: 344907-95-5
ethyl (E,E)-4-oxo-2-styrylbut-2-enoate

: 461640-95-9
(1S,2R)-1-amino-7-methyl-2,3-dihydro-1H-inden-2-ol

: 5-methyl-4-phenyl-1,9,9a,10a-tetrahydro-4H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene-2-carboxylic acid ethyl ester

: 461641-11-2
5-methyl-4-phenyl-1,9,9a,10a-tetrahydro-4H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene-2-carboxylic acid ethyl ester

Guidance literature:: In chloroform; at 24 ℃; for 3h;
DOI:10.1021/jo049381f

Reference yield:

: 2004-70-8,17410-45-6,25212-15-1,64940-84-7
1-methylbuta-1,3-diene

: 461641-11-2
5-methyl-4-phenyl-1,9,9a,10a-tetrahydro-4H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene-2-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: Pd/C / 200 °C

2.1: LiAlH₄ / diethyl ether / 0.17 h / 20 °C

3.1: 8.56 g / p-TsOH*H₂O / benzene / 0.5 h / 20 - 100 °C

4.1: aq. NaClO; Mn(III) complex of (S,S)-1,2-cyclohexanediamine derivative; 4-phenylpyridine N-oxide / 5 h / 20 °C

5.1: H₂SO₄; acetonitrile / hexane / 1 h / 20 °C

5.2: 52 percent / H₂O / 2 h / 100 °C

6.1: CHCl₃ / 3 h / 24 °C

With sodium hypochlorite; lithium aluminium tetrahydride; 4-Phenylpyridine 1-oxide; Mn(III) complex of (S,S)-1,2-cyclohexanediamine derivative; sulfuric acid; toluene-4-sulfonic acid; acetonitrile; palladium on activated charcoal; In diethyl ether; hexane; chloroform; benzene; 1.1: Diels-Alder reaction / 5.1: Jacobsen reaction / 6.1: Ritter reaction;
DOI:10.1021/jo049381f

Reference yield:

: 930-30-3
cyclopent-2-enone

: 461641-11-2
5-methyl-4-phenyl-1,9,9a,10a-tetrahydro-4H,4bH-10-oxa-4a-aza-indeno[1,2-a]indene-2-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: Pd/C / 200 °C

2.1: LiAlH₄ / diethyl ether / 0.17 h / 20 °C

3.1: 8.56 g / p-TsOH*H₂O / benzene / 0.5 h / 20 - 100 °C

4.1: aq. NaClO; Mn(III) complex of (S,S)-1,2-cyclohexanediamine derivative; 4-phenylpyridine N-oxide / 5 h / 20 °C

5.1: H₂SO₄; acetonitrile / hexane / 1 h / 20 °C

5.2: 52 percent / H₂O / 2 h / 100 °C

6.1: CHCl₃ / 3 h / 24 °C

With sodium hypochlorite; lithium aluminium tetrahydride; 4-Phenylpyridine 1-oxide; Mn(III) complex of (S,S)-1,2-cyclohexanediamine derivative; sulfuric acid; toluene-4-sulfonic acid; acetonitrile; palladium on activated charcoal; In diethyl ether; hexane; chloroform; benzene; 1.1: Diels-Alder reaction / 5.1: Jacobsen reaction / 6.1: Ritter reaction;
DOI:10.1021/jo049381f