methyl (R,E,E)-6-aza-5-benzyl-10-hydroxy-6-(p-toluenesulfonyl)deca-2,8-dienoate

Base Information

Chemical Name:methyl (R,E,E)-6-aza-5-benzyl-10-hydroxy-6-(p-toluenesulfonyl)deca-2,8-dienoate
CAS No.:1254356-60-9
Molecular Formula:C₂₄H₂₉NO₅S
Molecular Weight:443.564
Hs Code.:

Synonyms:methyl (R,E,E)-6-aza-5-benzyl-10-hydroxy-6-(p-toluenesulfonyl)deca-2,8-dienoate

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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 methyl (R,E,E)-6-aza-5-benzyl-10-hydroxy-6-(p-toluenesulfonyl)deca-2,8-dienoate

Chemical Property:

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Technology Process of methyl (R,E,E)-6-aza-5-benzyl-10-hydroxy-6-(p-toluenesulfonyl)deca-2,8-dienoate

There total 4 articles about methyl (R,E,E)-6-aza-5-benzyl-10-hydroxy-6-(p-toluenesulfonyl)deca-2,8-dienoate 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:

: 1254356-57-4
(S,E)-8-acetoxy-4-aza-3-benzyl-4-(p-toluenesulfonyl)oct-6-enenitrile

: 1254356-60-9
methyl (R,E,E)-6-aza-5-benzyl-10-hydroxy-6-(p-toluenesulfonyl)deca-2,8-dienoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: diisobutylaluminium hydride / dichloromethane; toluene / 2 h / -78 °C

1.2: 0.25 h / -78 - 20 °C

2.1: dichloromethane / 20 °C

With diisobutylaluminium hydride; In dichloromethane; toluene; 2.1: Wittig reaction;
DOI:10.1021/jo101631y

Reference yield:

: 3182-95-4
L-Phenylalaninol

: 1254356-60-9
methyl (R,E,E)-6-aza-5-benzyl-10-hydroxy-6-(p-toluenesulfonyl)deca-2,8-dienoate

Guidance literature:: Multi-step reaction with 5 steps

1.1: pyridine / dichloromethane

2.1: N,N-dimethyl-formamide

3.1: caesium carbonate / acetonitrile / 0.5 h / 20 °C

3.2: 12 h / 0 - 20 °C

4.1: diisobutylaluminium hydride / dichloromethane; toluene / 2 h / -78 °C

4.2: 0.25 h / -78 - 20 °C

5.1: dichloromethane / 20 °C

With pyridine; diisobutylaluminium hydride; caesium carbonate; In dichloromethane; N,N-dimethyl-formamide; toluene; acetonitrile; 5.1: Wittig reaction;
DOI:10.1021/jo101631y

Reference yield:

: 132161-97-8
(S)-N-(1-Cyano-3-phenylpropan-2-yl)-4-methylbenzenesulfonamide

: 1254356-60-9
methyl (R,E,E)-6-aza-5-benzyl-10-hydroxy-6-(p-toluenesulfonyl)deca-2,8-dienoate

Guidance literature:: Multi-step reaction with 3 steps

1.1: caesium carbonate / acetonitrile / 0.5 h / 20 °C

1.2: 12 h / 0 - 20 °C

2.1: diisobutylaluminium hydride / dichloromethane; toluene / 2 h / -78 °C

2.2: 0.25 h / -78 - 20 °C

3.1: dichloromethane / 20 °C

With diisobutylaluminium hydride; caesium carbonate; In dichloromethane; toluene; acetonitrile; 3.1: Wittig reaction;
DOI:10.1021/jo101631y