Benzaldehyde, 2-(1-phenylethoxy)-

Base Information

Chemical Name:Benzaldehyde, 2-(1-phenylethoxy)-
CAS No.:194418-21-8
Molecular Formula:C15H14O2
Molecular Weight:226.275
Hs Code.:
Mol file:194418-21-8.mol

Synonyms:

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Chemical Property of Benzaldehyde, 2-(1-phenylethoxy)-

Chemical Property:

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Technology Process of Benzaldehyde, 2-(1-phenylethoxy)-

There total 5 articles about Benzaldehyde, 2-(1-phenylethoxy)- 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: 72.0%

: N-(6-methylquinolin-8-yl)-2-(1-phenylethoxy)benzamide

: 194418-21-8
2-(1-phenylethoxy)benzaldehyde

Guidance literature:: With Schwartz's reagent; In tetrahydrofuran; at 20 ℃; for 6h; Schlenk technique; Inert atmosphere;
DOI:10.1002/anie.201913930

Reference yield:

: 98-85-1,13323-81-4
1-Phenylethanol

: 194418-21-8
2-(1-phenylethoxy)benzaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: 1-Adamantanecarboxylic acid; sodium 1-adamantanecarboxylate; tetrabutylammonium perchlorate; C₃₂H₂₁N₄NiO₂ / N,N-dimethyl acetamide / 12 h / 130 °C / Electrochemical reaction

2: Schwartz's reagent / tetrahydrofuran / 6 h / 20 °C / Schlenk technique; Inert atmosphere

With Schwartz's reagent; 1-Adamantanecarboxylic acid; C₃₂H₂₁N₄NiO₂; tetrabutylammonium perchlorate; sodium 1-adamantanecarboxylate; In tetrahydrofuran; N,N-dimethyl acetamide;
DOI:10.1002/anie.201913930

Reference yield:

: N-(6-methylquinolin-8-yl)benzamide

: 194418-21-8
2-(1-phenylethoxy)benzaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: (1,2-dimethoxyethane)dichloronickel(II); 1-Adamantanecarboxylic acid; sodium 1-adamantanecarboxylate; tetrabutylammonium perchlorate / N,N-dimethyl acetamide / 12 h / 130 °C / Inert atmosphere; Electrochemical reaction

2: Schwartz's reagent / tetrahydrofuran / 6 h / 20 °C / Schlenk technique; Inert atmosphere

With Schwartz's reagent; (1,2-dimethoxyethane)dichloronickel(II); 1-Adamantanecarboxylic acid; tetrabutylammonium perchlorate; sodium 1-adamantanecarboxylate; In tetrahydrofuran; N,N-dimethyl acetamide;
DOI:10.1002/anie.201913930