3-{[(4-fluoroanilino)oxo-sec-butyl-1λ⁶-sulfanylidene]amino}propanoic acid

Base Information

Chemical Name:3-{[(4-fluoroanilino)oxo-sec-butyl-1λ⁶-sulfanylidene]amino}propanoic acid
CAS No.:1520120-17-5
Molecular Formula:C₁₃H₁₉FN₂O₃S
Molecular Weight:302.37
Hs Code.:

3-{[(4-fluoroanilino)oxo-sec-butyl-1λ<sup>6</sup>-sulfanylidene]amino}propanoic acid

Synonyms:3-{[(4-fluoroanilino)oxo-sec-butyl-1λ⁶-sulfanylidene]amino}propanoic acid

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Chemical Property of 3-{[(4-fluoroanilino)oxo-sec-butyl-1λ⁶-sulfanylidene]amino}propanoic acid

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Technology Process of 3-{[(4-fluoroanilino)oxo-sec-butyl-1λ⁶-sulfanylidene]amino}propanoic acid

There total 4 articles about 3-{[(4-fluoroanilino)oxo-sec-butyl-1λ⁶-sulfanylidene]amino}propanoic acid 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%

: 1520119-89-4
ethyl 3-{[(4-fluoroanilino)oxo-sec-butyl-1λ⁶-sulfanylidene]amino}propanoate

: 1520120-17-5
3-{[(4-fluoroanilino)oxo-sec-butyl-1λ⁶-sulfanylidene]amino}propanoic acid

Guidance literature:: With lithium hydroxide; In tetrahydrofuran; water; Reflux;
DOI:10.1055/s-0033-1339760

Reference yield:

: 371-40-4
4-fluoroaniline

: 1520120-17-5
3-{[(4-fluoroanilino)oxo-sec-butyl-1λ⁶-sulfanylidene]amino}propanoic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: thionyl chloride / toluene / Reflux

2.1: tetrahydrofuran; diethyl ether / 0 °C / Inert atmosphere

3.1: tert-butylhypochlorite / tetrachloromethane / 1.5 h / 0 °C / Inert atmosphere

3.2: 12 h / 20 °C / Inert atmosphere

4.1: lithium hydroxide / water; tetrahydrofuran / Reflux

With thionyl chloride; tert-butylhypochlorite; lithium hydroxide; In tetrahydrofuran; tetrachloromethane; diethyl ether; water; toluene;
DOI:10.1055/s-0033-1339760

Reference yield:

: 52326-08-6
N-sulfinyl-4-fluoroaniline

: 1520120-17-5
3-{[(4-fluoroanilino)oxo-sec-butyl-1λ⁶-sulfanylidene]amino}propanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: tetrahydrofuran; diethyl ether / 0 °C / Inert atmosphere

2.1: tert-butylhypochlorite / tetrachloromethane / 1.5 h / 0 °C / Inert atmosphere

2.2: 12 h / 20 °C / Inert atmosphere

3.1: lithium hydroxide / water; tetrahydrofuran / Reflux

With tert-butylhypochlorite; lithium hydroxide; In tetrahydrofuran; tetrachloromethane; diethyl ether; water;
DOI:10.1055/s-0033-1339760