L-Pyroglutamic Acid → L-Pyroglutamic Acid

HRID 586699Notes

Reaction equation

HRID 586699 reaction equation
[NH:1]1[C:5](=[O:6])[CH2:4][CH2:3][C@H:2]1[C:7]([OH:9])=[O:8].[CH2:10]=[CH:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[CH2:18]=[CH:19][CH:20]=[CH2:21].CN(CCN(C)C)C.[Li]CCCC>CCCCCC>[NH:1]1[C:5](=[O:6])[CH2:4][CH2:3][C@H:2]1[C:7]([OH:9])=[O:8].[CH2:10]=[CH:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.[CH2:18]=[CH:19][CH:20]=[CH2:21]

Participants

8

Procedure

In this experiment, a 0.5/19.5/80 Pyr-AMS/styrene/1,3-butadiene terpolymer was prepared. The procedure described in Example 1 was used except that a premix containing Pyr-AMS, styrene and 1,3-butadiene in hexane at a weight ratio of 0.5:19.5:80 was used as the monomer premix solution and the molar ratio of potassium 3,7-dimethyl-3-octanoxide to TMEDA to n-BuLi was 0.015:2:1. The GC analysis of residual monomer again showed that polymerization rates of the three monomers were almost identical indicating that both Pyr-AMS and styrene were randomly distributed along the polymer chain.

Workup

  1. additionpremix solution
  2. customThe GC analysis of residual monomer again showed that polymerization rates of the three monomers

Sources & evidence

ORD record
ord-2137a05a766d47bfa07d132f8d5ae733
Source dataset
uspto-grants-2005_08
Patent number
US06936669B2

Reaction notes

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