HCID 12788654, compound → HCID 12788656, compound

HRID 1153827Notes

Reaction equation

HRID 1153827 reaction equation
C([O:3][C:4]([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][N:12]1[CH:18]([CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[C:16](=[O:17])[NH:15][C:13]1=[O:14])=[O:5])C.C(N1C(=O)C(CCCCCCCC)N(CCCCCCC(OCC)=O)C1=O)CCC>>[C:4]([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][N:12]1[CH:18]([CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[C:16](=[O:17])[NH:15][C:13]1=[O:14])([OH:5])=[O:3]

Participants

3

Reactant 2

HCID 12788654HCID 12788654, compoundHCID 20436978HCID 20436978, compound

Product 1

HCID 12788656HCID 12788656, compound

Procedure

By the method of Example 92, 1-(6-ethoxycarbonylhexyl)-5-octylhydantoin was converted into 3-butyl-1-(6-ethoxycarbonylhexyl)-5-octylhydantoin, which was hydrolysed to give 3-butyl-1-(6-carboxyhexyl-5-octylhydantoin as a colourless oil.

Sources & evidence

ORD record
ord-8b41a308a4a243518be3767ac41bf52a
Source dataset
uspto-grants-1984_12
Patent number
US04486443

Reaction notes

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