Phenol → M-Cresol

HRID 574051Notes

Reaction equation

HRID 574051 reaction equation
[ClH:1].[OH-].[Na+:3].[C:4]1([OH:10])[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[NH2:11][C@H:12]([C:19]([OH:21])=[O:20])[CH2:13][C:14]1[N:18]=[CH:17][NH:16][CH:15]=1>C([O-])(=O)C.[Zn+2].C([O-])(=O)C.OCC(CO)O>[C:4]1([OH:10])[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH:9]1[C:4]([OH:10])=[CH:5][CH:6]=[CH:7][C:8]=1[CH3:12].[Na+:3].[Cl-:1].[NH2:11][C@H:12]([C:19]([OH:21])=[O:20])[CH2:13][C:14]1[N:18]=[CH:17][NH:16][CH:15]=1

Participants

9

Procedure

An aqueous solution (Stock solution I) of phenol, m-cresol, glycerol and NaCl was prepared together with an aqueous solution (Stock solution II) of LysB29Nε-hexadecandioyl-γ-Glu desB30 human insulin. An aqueous solution (Stock solution III) of histidine was prepared and pH was adjusted to 7.4 using diluted HCl/NaOH. A fraction of Stock solution I was mixed with variable amounts of Stock solution III and a fraction of Stock solution II was added and pH was adjusted to about 7.5. An aqueous 10 mM zinc acetate solution was added in six equal portions, pH was adjusted to 7.4 using diluted HCl/NaOH and the solution was filtered through a 0.22 μm sterile filter.

Workup

  1. filtrationthe solution was filtered through a 0.22 μm sterile filter

Sources & evidence

ORD record
ord-d0d99fe55101451199125840bf044685
Source dataset
uspto-grants-2015_05
Patent number
US09034818B2

Reaction notes

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