HCID 20512462, compound → HCID 20512437, compound

HRID 894609Notes

Reaction equation

HRID 894609 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[N:9]1[CH2:13][CH:12]([CH2:14][C:15]([O:17]CC)=[O:16])[N:11]([C:20]2[C:25]([CH3:26])=[CH:24][CH:23]=[CH:22][C:21]=2[CH3:27])[C:10]1=[NH:28]>C(OCC)(=O)C>[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[N:9]1[CH2:13][CH:12]([CH2:14][C:15]([OH:17])=[O:16])[N:11]([C:20]2[C:21]([CH3:27])=[CH:22][CH:23]=[CH:24][C:25]=2[CH3:26])[C:10]1=[NH:28]

Participants

3

Reactant 1

HCID 20512462HCID 20512462, compound

Product 1

HCID 20512437HCID 20512437, compound

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

When the above product is allowed to stand at room temperature in ethyl acetate for 2 days, a transesterification reaction occurs, the ethyl 1,3-bis(2',6'-dimethylphenyl)-2-imino-imidazolidine-4-acetate, melting at 142°-144° C., is obtained.

Workup

  1. customa transesterification reaction

Sources & evidence

ORD record
ord-6b21813705544c0abdf48ea8aeeb2549
Source dataset
uspto-grants-1981_08
Patent number
US04284642

Reaction notes

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