4-(3-Acetylsulfanyl-2-tert-butoxycarbonylamino-propyl)-benzoic acid tert-butyl ester

Base Information

Chemical Name:4-(3-Acetylsulfanyl-2-tert-butoxycarbonylamino-propyl)-benzoic acid tert-butyl ester
CAS No.:156143-64-5
Molecular Formula:C₂₁H₃₁NO₅S
Molecular Weight:409.547
Hs Code.:

Synonyms:4-(3-Acetylsulfanyl-2-tert-butoxycarbonylamino-propyl)-benzoic acid tert-butyl ester

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Chemical Property of 4-(3-Acetylsulfanyl-2-tert-butoxycarbonylamino-propyl)-benzoic acid tert-butyl ester

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Technology Process of 4-(3-Acetylsulfanyl-2-tert-butoxycarbonylamino-propyl)-benzoic acid tert-butyl ester

There total 6 articles about 4-(3-Acetylsulfanyl-2-tert-butoxycarbonylamino-propyl)-benzoic acid tert-butyl ester 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: 66.0%

: 156143-63-4
4-(2-tert-Butoxycarbonylamino-3-hydroxy-propyl)-benzoic acid tert-butyl ester

: 507-09-5
tiolacetic acid

: 156143-64-5
4-(3-Acetylsulfanyl-2-tert-butoxycarbonylamino-propyl)-benzoic acid tert-butyl ester

Guidance literature:: With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; Ambient temperature;
DOI:10.1021/jm00035a014

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 156143-64-5
4-(3-Acetylsulfanyl-2-tert-butoxycarbonylamino-propyl)-benzoic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / dimethylformamide

2: 42 percent / NaBH₄ / ethanol; H₂O / 4 h / 50 °C

3: 66 percent / PPh₃, diisopropyl azodicarboxylate / tetrahydrofuran / Ambient temperature

With sodium tetrahydroborate; di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide;
DOI:10.1021/jm00035a014

Reference yield:

: 108052-76-2
4-(bromomethyl)benzoic acid 1,1-dimethylethyl ester

: 156143-64-5
4-(3-Acetylsulfanyl-2-tert-butoxycarbonylamino-propyl)-benzoic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 92 percent / KI, benzyltrimethylammonium hydroxide / dioxane; H₂O / 3 h / Ambient temperature

2: 50 percent / 1 N aq. HCl / diethyl ether / 4 h / Ambient temperature

3: 92 percent / dimethylformamide

4: 42 percent / NaBH₄ / ethanol; H₂O / 4 h / 50 °C

5: 66 percent / PPh₃, diisopropyl azodicarboxylate / tetrahydrofuran / Ambient temperature

With hydrogenchloride; sodium tetrahydroborate; di-isopropyl azodicarboxylate; N-benzyl-trimethylammonium hydroxide; triphenylphosphine; potassium iodide; In tetrahydrofuran; 1,4-dioxane; diethyl ether; ethanol; water; N,N-dimethyl-formamide;
DOI:10.1021/jm00035a014