N-[3-(3-Formyl-2-hydroxyphenoxy)propyl][(2,4,6-triisopropyl)benzene]sulfonamide

Base Information

Chemical Name:N-[3-(3-Formyl-2-hydroxyphenoxy)propyl][(2,4,6-triisopropyl)benzene]sulfonamide
CAS No.:273195-75-8
Molecular Formula:C₂₅H₃₅NO₅S
Molecular Weight:461.623
Hs Code.:

Synonyms:N-[3-(3-Formyl-2-hydroxyphenoxy)propyl][(2,4,6-triisopropyl)benzene]sulfonamide

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Chemical Property of N-[3-(3-Formyl-2-hydroxyphenoxy)propyl][(2,4,6-triisopropyl)benzene]sulfonamide

Chemical Property:

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Technology Process of N-[3-(3-Formyl-2-hydroxyphenoxy)propyl][(2,4,6-triisopropyl)benzene]sulfonamide

There total 3 articles about N-[3-(3-Formyl-2-hydroxyphenoxy)propyl][(2,4,6-triisopropyl)benzene]sulfonamide 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: 79.0%

: 273195-73-6
N-[3-[3-Formyl-2-(2-propenyloxy)phenoxy]propyl]-[(2,4,6-triisopropyl)benzene]sulfonamide

: 273195-75-8
N-[3-(3-Formyl-2-hydroxyphenoxy)propyl][(2,4,6-triisopropyl)benzene]sulfonamide

Guidance literature:: With formic acid; triethylamine; triphenylphosphine; palladium diacetate; In ethanol; for 2h; Heating;

Reference yield:

: 6553-96-4
2,4,6-triisopropylphenylsulfonyl chloride

: 273195-75-8
N-[3-(3-Formyl-2-hydroxyphenoxy)propyl][(2,4,6-triisopropyl)benzene]sulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: 91 percent / NEt₃ / CH₂Cl₂ / 11 h / 0 - 20 °C

2: 38 percent / K₂CO₃ / acetonitrile / 48 h / Heating

3: 79 percent / NEt₃; aq. HCOOH; PPh₃ / Pd(OAc)2 / ethanol / 2 h / Heating

With formic acid; potassium carbonate; triethylamine; triphenylphosphine; palladium diacetate; In ethanol; dichloromethane; acetonitrile; 1: Amination / 2: Etherification / 3: Deallylation;

Reference yield:

: 273195-71-4
N-(3-Chloropropyl)-[(2,4,6-triisopropyl)benzene]sulfonamide

: 273195-75-8
N-[3-(3-Formyl-2-hydroxyphenoxy)propyl][(2,4,6-triisopropyl)benzene]sulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: 38 percent / K₂CO₃ / acetonitrile / 48 h / Heating

2: 79 percent / NEt₃; aq. HCOOH; PPh₃ / Pd(OAc)2 / ethanol / 2 h / Heating

With formic acid; potassium carbonate; triethylamine; triphenylphosphine; palladium diacetate; In ethanol; acetonitrile; 1: Etherification / 2: Deallylation;