19340-88-6

Basic information

• Product Name: Butanamide, 4-hydroxy-N-(phenylmethyl)-
• CAS NO: 19340-88-6
• Molecular Formula: C11H15NO2
• Molecular Weight: 193.246
• Mol File: 19340-88-6.mol
• Article Data: 21

Chemical Properties

• CAS DataBase Reference: Butanamide, 4-hydroxy-N-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Butanamide, 4-hydroxy-N-(phenylmethyl)-(19340-88-6)
• EPA Substance Registry System: Butanamide, 4-hydroxy-N-(phenylmethyl)-(19340-88-6)

Safety Data

• Hazardous Substances Data: 19340-88-6(Hazardous Substances Data)

Upstream product

• 19340-86-4 N-benzyl-4-(benzyloxy)butanamide 
• 96-48-0 4-butanolide 
• 100-46-9 benzylamine 
• 110-63-4 Butane-1,4-diol 
• 925-57-5 methyl 4-hydroxybutanoate 
• 999-10-0 ethyl 4-hydroxybutanoate 
• 64984-60-7 4-oxo-4-[(phenylmethyl)amino]butanoic acid 
• 18406-59-2 N-benzyl-N,N-bis(trimethylsilyl)amine 
• 2142-06-5 1-(phenylmethyl)-2,5-pyrrolidinedione 
• 3287-99-8 benzylamine hydrochloride 
• 100446-71-7 N-benzyl-4-(trimethylsiloxy)butanamide 
• 2623-87-2 bromobutyric acid 
• 28341-54-0 4-(4-nitrophenoxy)butanoic acid 

Downstream Products

• 95564-68-4 Dihexyl-(γ-benzylcarbamoyl-propyl)-phosphat 
• 22813-61-2 N-benzyl-4-chlorobutanamide 
• 2142-06-5 1-(phenylmethyl)-2,5-pyrrolidinedione 
• 116614-85-8 ethyl (E)-2-(1-benzylpyrrolidin-2-ylidene)acetate 
• 17642-88-5 1-benzyl-2-pyrrolidinethione 
• 477952-41-3 6-[N-benzyl-N-(tert-butyloxycarbonyl)]amino-2-methyl-2-nitro-2-hexanone 
• 477952-40-2 6-[N-benzyl-N-(tert-butyloxycarbonyl)]amino-3-hydroxy-2-methyl-2-nitrohexane 
• 477952-43-5 (syn/anti)-6-[N-benzyl-N(tert-butyloxycarbonyl)]amino-2,4-dimethyl-2-nitro-3-hexanol 
• 477952-42-4 6-[N-benzyl-N-(tert-butyloxycarbonyl)]amino-2,4-dimethyl-2-nitro-2-hexanone 
• 213772-31-7 4-[N-benzyl-N-(tert-butyloxycarbonyl)]-amino-1-butanal 
• 117654-86-1 4-[N-(t-butoxycarbonyl)-N-[(phenyl)methyl]-amino]butan-1-ol 
• 59578-63-1 4-(benzylamino)-1-butanol 
• 19340-89-7 γ-Phenylacetoxy-buttersaeure-benzylamid 
• 5291-77-0 1-benzyl-2-pyrrolidone 

Relevant articles and documents

CATALYST FOR CONVERTING ESTER TO AMIDE USING HYDROXYL GROUP AS ORIENTATION GROUP

Provided is a method for amidating a hydroxy ester compound at a high chemical selectivity. The amidation reaction method for a hydroxy ester compound comprises, in the presence of a catalyst containing a compound of a transition metal of the group 4 or group 5 in the periodic table, reacting at least one kind of hydroxy ester compound selected from the group consisting of an α-hydroxy ester compound, a β-hydroxy ester compound, a γ-hydroxy ester compound and a δ-hydroxy ester compound with an amino compound so as to amidate an ester group having a hydroxyl group at the α-, β-, γ- or δ-position of the hydroxy ester compound.

Preparation method of hydroxyamide

The invention discloses a preparation method of a hydroxyamide shown as formula (I). The hydroxyamide is prepared through homogeneous catalytic hydrogenation reaction of a cyclic imide represented byformula (II), wherein R1, R2 and R3 are respectively and