benzyl 2-(benzyloxy)-5-(2-(4-(tert-butoxycarbonylamino)butanoyloxy)acetyl)benzoate

Base Information

Chemical Name:benzyl 2-(benzyloxy)-5-(2-(4-(tert-butoxycarbonylamino)butanoyloxy)acetyl)benzoate
CAS No.:1292299-07-0
Molecular Formula:C₃₂H₃₅NO₈
Molecular Weight:561.632
Hs Code.:

Synonyms:benzyl 2-(benzyloxy)-5-(2-(4-(tert-butoxycarbonylamino)butanoyloxy)acetyl)benzoate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of benzyl 2-(benzyloxy)-5-(2-(4-(tert-butoxycarbonylamino)butanoyloxy)acetyl)benzoate

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Technology Process of benzyl 2-(benzyloxy)-5-(2-(4-(tert-butoxycarbonylamino)butanoyloxy)acetyl)benzoate

There total 2 articles about benzyl 2-(benzyloxy)-5-(2-(4-(tert-butoxycarbonylamino)butanoyloxy)acetyl)benzoate 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: 75.0%

: 57294-38-9
N-(tert-butoxycarbonyl)-4-aminobutanoic acid

: 943969-36-6
benzyl 2-(benzyloxy)-5-(2-bromoacetyl)benzoate

: 1292299-07-0
benzyl 2-(benzyloxy)-5-(2-(4-(tert-butoxycarbonylamino)butanoyloxy)acetyl)benzoate

Guidance literature:: With potassium carbonate; In acetonitrile; at 20 ℃;
DOI:10.1139/V10-143

Reference yield:

: 1292299-06-9
benzyl 5-acetyl-2-(benzyloxy)benzoate

: 1292299-07-0
benzyl 2-(benzyloxy)-5-(2-(4-(tert-butoxycarbonylamino)butanoyloxy)acetyl)benzoate

Guidance literature:: Multi-step reaction with 2 steps

1: phenyltrimethylammonium tribromide / methanol; dichloromethane / 20 °C

2: potassium carbonate / acetonitrile / 20 °C

With phenyltrimethylammonium tribromide; potassium carbonate; In methanol; dichloromethane; acetonitrile;
DOI:10.1139/V10-143