(4-tert-butoxycarbonylmethylsulfanyl-2,5-dichloro-phenylsulfanyl)-acetic acid

Base Information

Chemical Name:(4-tert-butoxycarbonylmethylsulfanyl-2,5-dichloro-phenylsulfanyl)-acetic acid
CAS No.:415926-82-8
Molecular Formula:C₁₄H₁₆Cl₂O₄S₂
Molecular Weight:383.317
Hs Code.:

(4-<i>tert</i>-butoxycarbonylmethylsulfanyl-2,5-dichloro-phenylsulfanyl)-acetic acid

Synonyms:(4-tert-butoxycarbonylmethylsulfanyl-2,5-dichloro-phenylsulfanyl)-acetic acid

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Chemical Property of (4-tert-butoxycarbonylmethylsulfanyl-2,5-dichloro-phenylsulfanyl)-acetic acid

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Technology Process of (4-tert-butoxycarbonylmethylsulfanyl-2,5-dichloro-phenylsulfanyl)-acetic acid

There total 6 articles about (4-tert-butoxycarbonylmethylsulfanyl-2,5-dichloro-phenylsulfanyl)-acetic 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: 95.0%

: 208512-70-3
(2,5-dichloro-4-methoxycarbonylmethylsulfanyl-phenylsulfanyl)-acetic acid tert-butyl ester

: 415926-82-8
(4-tert-butoxycarbonylmethylsulfanyl-2,5-dichloro-phenylsulfanyl)-acetic acid

Guidance literature:: With sodium hydroxide; In tetrahydrofuran; at 20 ℃; for 0.666667h;
DOI:10.1016/S0968-0896(02)00335-8

Reference yield:

: 5292-43-3
bromoacetic acid tert-butyl ester

: 415926-82-8
(4-tert-butoxycarbonylmethylsulfanyl-2,5-dichloro-phenylsulfanyl)-acetic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 94 percent / Et₃N / CH₂Cl₂ / 1.33 h / cooling

2: 67 percent / m-chloroperbenzoic acid / CHCl₃ / 2.5 h / 0 - 20 °C

3: 75 percent / dimethylformamide / 0.83 h / 20 °C

4: 87 percent / NaI; (CF₃CO)2O / acetone / 1 h / 20 °C

5: 95 percent / aq. NaOH / tetrahydrofuran / 0.67 h / 20 °C

With sodium hydroxide; triethylamine; 3-chloro-benzenecarboperoxoic acid; trifluoroacetic anhydride; sodium iodide; In tetrahydrofuran; dichloromethane; chloroform; N,N-dimethyl-formamide; acetone;
DOI:10.1016/S0968-0896(02)00335-8

Reference yield:

: 3773-14-6
2,4,5-trichlorothiophenol

: 415926-82-8
(4-tert-butoxycarbonylmethylsulfanyl-2,5-dichloro-phenylsulfanyl)-acetic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 94 percent / Et₃N / CH₂Cl₂ / 1.33 h / cooling

2: 67 percent / m-chloroperbenzoic acid / CHCl₃ / 2.5 h / 0 - 20 °C

3: 75 percent / dimethylformamide / 0.83 h / 20 °C

4: 87 percent / NaI; (CF₃CO)2O / acetone / 1 h / 20 °C

5: 95 percent / aq. NaOH / tetrahydrofuran / 0.67 h / 20 °C

With sodium hydroxide; triethylamine; 3-chloro-benzenecarboperoxoic acid; trifluoroacetic anhydride; sodium iodide; In tetrahydrofuran; dichloromethane; chloroform; N,N-dimethyl-formamide; acetone;
DOI:10.1016/S0968-0896(02)00335-8