HCID 12788654, compound → HCID 20436819, compound

HRID 444041Notes

Reaction equation

HRID 444041 reaction equation
C(OC(CCCCCCN1C(CCCCCCCC)C(=O)NC1=O)=O)C.[CH2:27]([N:31]1[C:35](=[O:36])[CH:34]([CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH3:44])[N:33]([CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH2:50][C:51]([O:53]CC)=[O:52])[C:32]1=[O:56])[CH2:28][CH2:29][CH3:30]>>[CH2:27]([N:31]1[C:35](=[O:36])[CH:34]([CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH3:44])[N:33]([CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH2:50][C:51]([OH:53])=[O:52])[C:32]1=[O:56])[CH2:28][CH2:29][CH3:30]

Participants

3

Reactant 2

HCID 12788654HCID 12788654, compoundHCID 20436978HCID 20436978, compound

Product 1

HCID 20436819HCID 20436819, 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-c39ba7335bb441fcaec3a31c02278996
Source dataset
uspto-grants-1981_04
Patent number
US04262128

Reaction notes

Loading…