Z-MeA2bu(γPht)-O-tBu

Base Information

Chemical Name:Z-MeA2bu(γPht)-O-tBu
CAS No.:117194-43-1
Molecular Formula:C₂₅H₂₈N₂O₆
Molecular Weight:452.507
Hs Code.:

Synonyms:

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Chemical Property of Z-MeA2bu(γPht)-O-tBu

Chemical Property:

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Technology Process of Z-MeA2bu(γPht)-O-tBu

There total 6 articles about Z-MeA2bu(γPht)-O-tBu 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:

: 84-66-2
Diethyl phthalate

: 117194-43-1
Z-MeA2bu(γPht)-O-tBu

Guidance literature:: Multi-step reaction with 5 steps

1: 67 percent / acetonitrile / 48 h / Ambient temperature

2: 100 percent / TsOH*H₂O / toluene / 1 h / Heating

3: 100 percent / Et₃SiH / trifluoroacetic acid; CHCl₃ / 24 h / Ambient temperature

4: 81 percent / HBr / acetic acid / 1 h / Ambient temperature

5: H₂SO₄ / CH₂Cl₂

With triethylsilane; sulfuric acid; hydrogen bromide; toluene-4-sulfonic acid; In dichloromethane; chloroform; acetic acid; toluene; acetonitrile; trifluoroacetic acid;

Reference yield:

: 1155-62-0
N-benzyloxycarbonyl-L-glutamic acid

: 117194-43-1
Z-MeA2bu(γPht)-O-tBu

Guidance literature:: Multi-step reaction with 6 steps

1: 103 percent / (CF₃COO)2-I-Ph, pyridine / 24 h / Ambient temperature

2: 67 percent / acetonitrile / 48 h / Ambient temperature

3: 100 percent / TsOH*H₂O / toluene / 1 h / Heating

4: 100 percent / Et₃SiH / trifluoroacetic acid; CHCl₃ / 24 h / Ambient temperature

5: 81 percent / HBr / acetic acid / 1 h / Ambient temperature

6: H₂SO₄ / CH₂Cl₂

With pyridine; triethylsilane; sulfuric acid; hydrogen bromide; toluene-4-sulfonic acid; bis-[(trifluoroacetoxy)iodo]benzene; In dichloromethane; chloroform; acetic acid; toluene; acetonitrile; trifluoroacetic acid;

Reference yield:

: 62234-40-6
(2S)-2-{[(benzyloxy)carbonyl]amino}-4-(dimethylamino)butanoic acid

: 117194-43-1
Z-MeA2bu(γPht)-O-tBu

Guidance literature:: Multi-step reaction with 5 steps

1: 67 percent / acetonitrile / 48 h / Ambient temperature

2: 100 percent / TsOH*H₂O / toluene / 1 h / Heating

3: 100 percent / Et₃SiH / trifluoroacetic acid; CHCl₃ / 24 h / Ambient temperature

4: 81 percent / HBr / acetic acid / 1 h / Ambient temperature

5: H₂SO₄ / CH₂Cl₂

With triethylsilane; sulfuric acid; hydrogen bromide; toluene-4-sulfonic acid; In dichloromethane; chloroform; acetic acid; toluene; acetonitrile; trifluoroacetic acid;