4-(Hydroxyamino)-4-oxobutanoic acid

4-(Hydroxyamino)-4-oxobutanoic acid Structure
CAS No.
4743-99-1
Chemical Name:
4-(Hydroxyamino)-4-oxobutanoic acid
Synonyms
Tofacitinib Impurity 208;N-Hydroxysuccinamidic acid;4-(Hydroxyamino)-4-oxobutanoic acid;Butanoic acid, 4-(hydroxyamino)-4-oxo-;3-(Hydroxyaminocarbonyl)propionic acid
CBNumber:
CB02174169
Molecular Formula:
C4H7NO4
Molecular Weight:
133.1
MOL File:
4743-99-1.mol
Modify Date:
2022/8/26 12:15:11

4-(Hydroxyamino)-4-oxobutanoic acid Properties

Melting point 82-86 °C(Solv: acetonitrile (75-05-8))
Density 1.436±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,Store in freezer, under -20°C
pka 5.28±0.10(Predicted)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338

4-(Hydroxyamino)-4-oxobutanoic acid Chemical Properties,Uses,Production

Preparation

To a refluxing solution of 5.0 gm (0.05 mole) of succinic anhydride in 100 ml of benzene is added a solution of 6.3 gm (0.05 mole) of O-ben- zylhydroxylamine in 20 ml of benzene. As soon as the addition has been completed, the reaction mixture is cooled, and the precipitated product is separated. Upon recrystallization from a benzene-methyl ethyl ketone mixture, 7.6 gm (68.2%) of N-benzyloxysuccinamic acid, m.p. 95-96°C isolated.
A suspension of 4.3 gm (0.0193 mole) of this intermediate and a stron- tium carbonate catalyst containing 5% palladium in methyl ethyl ketone is hydrogenated. Upon working up the reaction mixture, 1.45 gm (56.7%) of succinomonohydroxamic acid, m.p. 95-96°C is isolated.
Preparation of N-Hydroxysuccinamic Acid

4-(Hydroxyamino)-4-oxobutanoic acid Preparation Products And Raw materials

Raw materials

Preparation Products

4-(Hydroxyamino)-4-oxobutanoic acid Suppliers

3-(Hydroxyaminocarbonyl)propionic acid 4-(Hydroxyamino)-4-oxobutanoic acid N-Hydroxysuccinamidic acid Butanoic acid, 4-(hydroxyamino)-4-oxo- Tofacitinib Impurity 208 4743-99-1