HCID 22761697, compound → HCID 22761721, compound

HRID 1834048Notes

Reaction equation

HRID 1834048 reaction equation
[N+:1]([C:4]1[O:5][C:6]2[C:18]([C:19]([NH:21][CH2:22][C:23]([O:25]CC)=[O:24])=[O:20])=[CH:17][CH:16]=[CH:15][C:7]=2[C:8]=1[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)([O-:3])=[O:2]>[OH-].[Na+]>[N+:1]([C:4]1[O:5][C:6]2[C:18]([C:19]([NH:21][CH2:22][C:23]([OH:25])=[O:24])=[O:20])=[CH:17][CH:16]=[CH:15][C:7]=2[C:8]=1[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)([O-:3])=[O:2]

Participants

3

Reactant 1

HCID 22761697HCID 22761697, compound

Product 1

HCID 22761721HCID 22761721, compound

Reagents, catalysts & solvents 1

HCID 14798Sodium HydroxideSolvent

Procedure

Ethyl N-(2-nitro-3-phenyl-7-benzofuranoyl)glycinate is hydrolyzed by stirring in ethanolic sodium hydroxide solution to provide N-(2-nitro-3-phenyl-7-benzofuranoyl)glycine, m.p. 123°-126° C.

Sources & evidence

ORD record
ord-f1093ef87f3741e0b65be5aaf96e86a9
Source dataset
uspto-grants-1978_01
Patent number
US04067993

Reaction notes

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