[9-(4-Methoxy-benzenesulfonyl)-4-oxo-2,3,4,9-tetrahydro-1H-carbazol-2-yl]-acetic acid methyl ester

Base Information

Chemical Name:[9-(4-Methoxy-benzenesulfonyl)-4-oxo-2,3,4,9-tetrahydro-1H-carbazol-2-yl]-acetic acid methyl ester
CAS No.:137333-39-2
Molecular Formula:C₂₂H₂₁NO₆S
Molecular Weight:427.478
Hs Code.:

Synonyms:[9-(4-Methoxy-benzenesulfonyl)-4-oxo-2,3,4,9-tetrahydro-1H-carbazol-2-yl]-acetic acid methyl ester

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Chemical Property of [9-(4-Methoxy-benzenesulfonyl)-4-oxo-2,3,4,9-tetrahydro-1H-carbazol-2-yl]-acetic acid methyl ester

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Technology Process of [9-(4-Methoxy-benzenesulfonyl)-4-oxo-2,3,4,9-tetrahydro-1H-carbazol-2-yl]-acetic acid methyl ester

There total 5 articles about [9-(4-Methoxy-benzenesulfonyl)-4-oxo-2,3,4,9-tetrahydro-1H-carbazol-2-yl]-acetic acid methyl 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:

: 137333-34-7,137333-35-8,39762-51-1
(3-Oxo-cyclohexyl)-acetic Acid

: 137333-39-2
[9-(4-Methoxy-benzenesulfonyl)-4-oxo-2,3,4,9-tetrahydro-1H-carbazol-2-yl]-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 73 percent / aq. acetic acid / 10 h / Heating

2: 99.6 percent / concd HCl, dimethoxypropane / 2 h / 20 °C

3: 85 percent / dichlorodicyanoquinone / tetrahydrofuran; H₂O / 2 h / 0 °C

4: tetra-N-benzylammonium chloride, 30percent NaOH / CH₂Cl₂ / 1 h

With hydrogenchloride; sodium hydroxide; Bn₄NCl; dimethoxypropane; acetic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; dichloromethane; water;
DOI:10.1021/jo00027a016

Reference yield:

: 59-88-1
phenylhydrazine hydrochloride

: 137333-39-2
[9-(4-Methoxy-benzenesulfonyl)-4-oxo-2,3,4,9-tetrahydro-1H-carbazol-2-yl]-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 73 percent / aq. acetic acid / 10 h / Heating

2: 99.6 percent / concd HCl, dimethoxypropane / 2 h / 20 °C

3: 85 percent / dichlorodicyanoquinone / tetrahydrofuran; H₂O / 2 h / 0 °C

4: tetra-N-benzylammonium chloride, 30percent NaOH / CH₂Cl₂ / 1 h

With hydrogenchloride; sodium hydroxide; Bn₄NCl; dimethoxypropane; acetic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; dichloromethane; water;
DOI:10.1021/jo00027a016

Reference yield:

: 137333-36-9
1,2,3,4-tetrahydro-9H-carbazole-2-acetic acid

: 137333-39-2
[9-(4-Methoxy-benzenesulfonyl)-4-oxo-2,3,4,9-tetrahydro-1H-carbazol-2-yl]-acetic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 99.6 percent / concd HCl, dimethoxypropane / 2 h / 20 °C

2: 85 percent / dichlorodicyanoquinone / tetrahydrofuran; H₂O / 2 h / 0 °C

3: tetra-N-benzylammonium chloride, 30percent NaOH / CH₂Cl₂ / 1 h

With hydrogenchloride; sodium hydroxide; Bn₄NCl; dimethoxypropane; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; dichloromethane; water;
DOI:10.1021/jo00027a016