N-[(E)-3-(3-ⁿbutoxy-3-oxoprop-1-en-1-yl)thenoyl]-S-methyl-S-phenylsulfoximine

Base Information

Chemical Name:N-[(E)-3-(3-ⁿbutoxy-3-oxoprop-1-en-1-yl)thenoyl]-S-methyl-S-phenylsulfoximine
CAS No.:1616088-46-0
Molecular Formula:C₁₇H₁₆ClNO₄S₂
Molecular Weight:397.903
Hs Code.:

N-[(E)-3-(3-<sup>n</sup>butoxy-3-oxoprop-1-en-1-yl)thenoyl]-S-methyl-S-phenylsulfoximine

Synonyms:N-[(E)-3-(3-ⁿbutoxy-3-oxoprop-1-en-1-yl)thenoyl]-S-methyl-S-phenylsulfoximine

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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 N-[(E)-3-(3-ⁿbutoxy-3-oxoprop-1-en-1-yl)thenoyl]-S-methyl-S-phenylsulfoximine

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Technology Process of N-[(E)-3-(3-ⁿbutoxy-3-oxoprop-1-en-1-yl)thenoyl]-S-methyl-S-phenylsulfoximine

There total 3 articles about N-[(E)-3-(3-ⁿbutoxy-3-oxoprop-1-en-1-yl)thenoyl]-S-methyl-S-phenylsulfoximine 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: 85.0%

: 1616087-95-6
N-[5-chlorothenoyl]-S-methyl-S-phenylsulfoximine

: 140-88-5,9003-32-1
ethyl acrylate

: 1616088-46-0
N-[(E)-3-(3-ⁿbutoxy-3-oxoprop-1-en-1-yl)thenoyl]-S-methyl-S-phenylsulfoximine

Guidance literature:: With silver tetrafluoroborate; [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂; copper(II) acetate hydrate; In 1,2-dichloro-ethane; at 120 ℃; for 24h; regioselective reaction; Inert atmosphere; Glovebox; Schlenk technique;
DOI:10.1021/jo5008465

Reference yield:

: 4381-25-3
S-methyl-S-phenylsulfoximine

: 1616088-46-0
N-[(E)-3-(3-ⁿbutoxy-3-oxoprop-1-en-1-yl)thenoyl]-S-methyl-S-phenylsulfoximine

Guidance literature:: Multi-step reaction with 2 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 12 h / 0 - 20 °C / Inert atmosphere; Schlenk technique

2: [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂; copper(II) acetate hydrate; silver tetrafluoroborate / 1,2-dichloro-ethane / 24 h / 120 °C / Inert atmosphere; Glovebox; Schlenk technique

With dmap; silver tetrafluoroborate; [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂; copper(II) acetate hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; 1,2-dichloro-ethane;
DOI:10.1021/jo5008465

Reference yield:

: 1193-82-4
racemic methyl phenyl sulfoxide

: 1616088-46-0
N-[(E)-3-(3-ⁿbutoxy-3-oxoprop-1-en-1-yl)thenoyl]-S-methyl-S-phenylsulfoximine

Guidance literature:: Multi-step reaction with 3 steps

1: sodium azide; sulfuric acid / chloroform / Schlenk technique

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 12 h / 0 - 20 °C / Inert atmosphere; Schlenk technique

3: [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂; copper(II) acetate hydrate; silver tetrafluoroborate / 1,2-dichloro-ethane / 24 h / 120 °C / Inert atmosphere; Glovebox; Schlenk technique

With dmap; silver tetrafluoroborate; sodium azide; [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂; copper(II) acetate hydrate; sulfuric acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; chloroform; 1,2-dichloro-ethane;
DOI:10.1021/jo5008465