5-(2-(4-(tert-butoxycarbonylamino)butanoyloxy)acetyl)-2-hydroxybenzoic acid

Base Information

Chemical Name:5-(2-(4-(tert-butoxycarbonylamino)butanoyloxy)acetyl)-2-hydroxybenzoic acid
CAS No.:1292299-08-1
Molecular Formula:C₁₈H₂₃NO₈
Molecular Weight:381.383
Hs Code.:

Synonyms:5-(2-(4-(tert-butoxycarbonylamino)butanoyloxy)acetyl)-2-hydroxybenzoic acid

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Chemical Property of 5-(2-(4-(tert-butoxycarbonylamino)butanoyloxy)acetyl)-2-hydroxybenzoic acid

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Technology Process of 5-(2-(4-(tert-butoxycarbonylamino)butanoyloxy)acetyl)-2-hydroxybenzoic acid

There total 3 articles about 5-(2-(4-(tert-butoxycarbonylamino)butanoyloxy)acetyl)-2-hydroxybenzoic 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: 96.0%

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

: 1292299-08-1
5-(2-(4-(tert-butoxycarbonylamino)butanoyloxy)acetyl)-2-hydroxybenzoic acid

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In ethyl acetate; at 20 ℃;
DOI:10.1139/V10-143

Reference yield:

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

: 1292299-08-1
5-(2-(4-(tert-butoxycarbonylamino)butanoyloxy)acetyl)-2-hydroxybenzoic acid

Guidance literature:: Multi-step reaction with 3 steps

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

2: potassium carbonate / acetonitrile / 20 °C

3: palladium 10% on activated carbon; hydrogen / ethyl acetate / 20 °C

With palladium 10% on activated carbon; hydrogen; phenyltrimethylammonium tribromide; potassium carbonate; In methanol; dichloromethane; ethyl acetate; acetonitrile;
DOI:10.1139/V10-143

Reference yield:

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

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

: 1292299-08-1
5-(2-(4-(tert-butoxycarbonylamino)butanoyloxy)acetyl)-2-hydroxybenzoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / acetonitrile / 20 °C

2: palladium 10% on activated carbon; hydrogen / ethyl acetate / 20 °C

With palladium 10% on activated carbon; hydrogen; potassium carbonate; In ethyl acetate; acetonitrile;
DOI:10.1139/V10-143