Benzyl-[4-benzyloxy-3-(2-oxo-2-phenyl-ethylsulfanyl)-butyl]-carbamic acid tert-butyl ester

Base Information

Chemical Name:Benzyl-[4-benzyloxy-3-(2-oxo-2-phenyl-ethylsulfanyl)-butyl]-carbamic acid tert-butyl ester
CAS No.:208585-90-4
Molecular Formula:C₃₁H₃₇NO₄S
Molecular Weight:519.705
Hs Code.:

Synonyms:Benzyl-[4-benzyloxy-3-(2-oxo-2-phenyl-ethylsulfanyl)-butyl]-carbamic acid tert-butyl ester

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Chemical Property of Benzyl-[4-benzyloxy-3-(2-oxo-2-phenyl-ethylsulfanyl)-butyl]-carbamic acid tert-butyl ester

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Technology Process of Benzyl-[4-benzyloxy-3-(2-oxo-2-phenyl-ethylsulfanyl)-butyl]-carbamic acid tert-butyl ester

There total 7 articles about Benzyl-[4-benzyloxy-3-(2-oxo-2-phenyl-ethylsulfanyl)-butyl]-carbamic 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:

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

: 208585-90-4
Benzyl-[4-benzyloxy-3-(2-oxo-2-phenyl-ethylsulfanyl)-butyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 99 percent / K₂CO₃ / dioxane; H₂O

2: 1.) diisopropylazodicarboxylate, Ph₃P / 1.) THF, 1 h, 2.) THF, overnight

3: K₂CO₃, MeOH

With methanol; di-isopropyl azodicarboxylate; potassium carbonate; triphenylphosphine; In 1,4-dioxane; water;
DOI:10.1021/ja973464e

Reference yield:

: 14593-43-2
benzyl allyl ether

: 208585-90-4
Benzyl-[4-benzyloxy-3-(2-oxo-2-phenyl-ethylsulfanyl)-butyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 74 percent / benzene / 25 h / Heating

2: 72 percent / NiCl₂, LiAlH₄ / tetrahydrofuran / 10 h / Ambient temperature

3: 99 percent / K₂CO₃ / dioxane; H₂O

4: 1.) diisopropylazodicarboxylate, Ph₃P / 1.) THF, 1 h, 2.) THF, overnight

5: K₂CO₃, MeOH

With methanol; lithium aluminium tetrahydride; di-isopropyl azodicarboxylate; potassium carbonate; triphenylphosphine; nickel dichloride; In tetrahydrofuran; 1,4-dioxane; water; benzene;
DOI:10.1021/ja973464e

Reference yield:

: 74635-18-0
N-benzylmethylene nitrone

: 208585-90-4
Benzyl-[4-benzyloxy-3-(2-oxo-2-phenyl-ethylsulfanyl)-butyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 74 percent / benzene / 25 h / Heating

2: 72 percent / NiCl₂, LiAlH₄ / tetrahydrofuran / 10 h / Ambient temperature

3: 99 percent / K₂CO₃ / dioxane; H₂O

4: 1.) diisopropylazodicarboxylate, Ph₃P / 1.) THF, 1 h, 2.) THF, overnight

5: K₂CO₃, MeOH

With methanol; lithium aluminium tetrahydride; di-isopropyl azodicarboxylate; potassium carbonate; triphenylphosphine; nickel dichloride; In tetrahydrofuran; 1,4-dioxane; water; benzene;
DOI:10.1021/ja973464e