HCID 11075036, compound → HCID 131716796, compound

HRID 981762Notes

Reaction equation

HRID 981762 reaction equation
C([O:8][C:9](=[O:16])[C@@H:10]([CH2:12][C:13]([OH:15])=[O:14])[OH:11])C1C=CC=CC=1.Cl.[C:18]([O:24]N)(=[O:23])[C:19]([CH3:22])([CH3:21])[CH3:20]>>[C:18]([O:24][O:8][C:9](=[O:16])[C@@H:10]([CH2:12][C:13]([OH:15])=[O:14])[OH:11])(=[O:23])[C:19]([CH3:22])([CH3:21])[CH3:20]

Participants

3

Reactant 2

HCID 11075036HCID 11075036, compoundHCID 136754571-(Aminooxy)-2,2-dimethylpropan-1-one--hydrogen chloride (1/1)

Product 1

HCID 131716796HCID 131716796, compoundYield 89%

Procedure

D-Malic acid monobenzyl ester prepared as described by Example 1A was allowed to react with pivalyloxyamine hydrochloride according to the method described in the preceding examples (Part B) to provide in 89% yield O-pivalyloxy-D-malic acid hydroxyamate monobenzyl ester melting at about 75° to about 76° C.

Sources & evidence

ORD record
ord-a99727a42dcf4177b9c4ee7e013ee958
Source dataset
uspto-grants-1991_02
Patent number
US04992544

Reaction notes

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