rac-2-Allyloxy-2-phenylpent-4-enal

Base Information

Chemical Name:rac-2-Allyloxy-2-phenylpent-4-enal
CAS No.:308141-30-2
Molecular Formula:C₁₄H₁₆O₂
Molecular Weight:216.28
Hs Code.:

Synonyms:rac-2-Allyloxy-2-phenylpent-4-enal

Suppliers and Price of rac-2-Allyloxy-2-phenylpent-4-enal

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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 rac-2-Allyloxy-2-phenylpent-4-enal

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Technology Process of rac-2-Allyloxy-2-phenylpent-4-enal

There total 3 articles about rac-2-Allyloxy-2-phenylpent-4-enal 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: 67.0%

: 308141-25-5
rac-2-Allyloxy-2-phenylpent-4-en-1-ol

: 308141-30-2
rac-2-Allyloxy-2-phenylpent-4-enal

Guidance literature:: With dipyridinium dichromate; In dichloromethane; at 20 ℃; for 24h;
DOI:10.1039/b004302h

Reference yield:

: 4358-87-6
(RS)-methyl mandelate

: 308141-30-2
rac-2-Allyloxy-2-phenylpent-4-enal

Guidance literature:: Multi-step reaction with 3 steps

1: 44 percent

2: 78 percent / DIBAL-H / diethyl ether / 1 h / 20 °C

3: 67 percent / PDC / CH₂Cl₂ / 24 h / 20 °C

With dipyridinium dichromate; diisobutylaluminium hydride; In diethyl ether; dichloromethane; 2: Reduction / 3: Oxidation;
DOI:10.1039/b004302h

Reference yield:

: 308141-18-6
rac-2-Allyloxy-2-phenylpent-4-enoic acid methyl ester

: 308141-30-2
rac-2-Allyloxy-2-phenylpent-4-enal

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / DIBAL-H / diethyl ether / 1 h / 20 °C

2: 67 percent / PDC / CH₂Cl₂ / 24 h / 20 °C

With dipyridinium dichromate; diisobutylaluminium hydride; In diethyl ether; dichloromethane; 1: Reduction / 2: Oxidation;
DOI:10.1039/b004302h