C₃₄H₂₉N

Base Information

Chemical Name:C₃₄H₂₉N
CAS No.:1447801-16-2
Molecular Formula:C₃₄H₂₉N
Molecular Weight:451.611
Hs Code.:

Synonyms:

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₃₄H₂₉N

Chemical Property:

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Technology Process of C₃₄H₂₉N

There total 3 articles about C₃₄H₂₉N 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: 61.3%

: C₂₆H₂₄O

: 1137-94-6
1-(2-phenyl-2-oxoethyl)pyridinium iodide

: 1447801-16-2
C₃₄H₂₉N

Guidance literature:: With ammonium acetate; acetic acid; In methanol; Reflux;
DOI:10.1002/anie.201301149

Reference yield:

: 86-73-7
9H-fluorene

: 1447801-16-2
C₃₄H₂₉N

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium tert-butylate / tetrahydrofuran / Inert atmosphere; Reflux

2.1: carbon disulfide; aluminum (III) chloride / 3 h / Inert atmosphere; Reflux

3.1: sodium hydroxide / methanol / 0.17 h

3.2: 60 °C

4.1: ammonium acetate; acetic acid / methanol / Reflux

With carbon disulfide; aluminum (III) chloride; potassium tert-butylate; ammonium acetate; acetic acid; sodium hydroxide; In tetrahydrofuran; methanol;
DOI:10.1002/anie.201301149

Reference yield:

: 2294-79-3
9,9-diethyl-9H-fluorene

: 1447801-16-2
C₃₄H₂₉N

Guidance literature:: Multi-step reaction with 3 steps

1.1: carbon disulfide; aluminum (III) chloride / 3 h / Inert atmosphere; Reflux

2.1: sodium hydroxide / methanol / 0.17 h

2.2: 60 °C

3.1: ammonium acetate; acetic acid / methanol / Reflux

With carbon disulfide; aluminum (III) chloride; ammonium acetate; acetic acid; sodium hydroxide; In methanol;
DOI:10.1002/anie.201301149