HCID 12788654, compound → HCID 20436819, compound

HRID 1395593Notes

Reaction equation

HRID 1395593 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 40, 1-(6-ethoxycarbonylhexyl)-5-octylhydantoin (see Example 36) 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-7e597a0f23074b87b6f25fede36675c2
Source dataset
uspto-grants-1980_05
Patent number
US04204068

Reaction notes

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