December 23, 2024, 09:41:23 AM
Forum Rules: Read This Before Posting


Topic: Organic chemistry - specific derivatization of tertiary alcohol  (Read 1980 times)

0 Members and 2 Guests are viewing this topic.

Offline Jall

  • Very New Member
  • *
  • Posts: 2
  • Mole Snacks: +0/-0
Hello,

I'm actually working on a project about graphite oxide (GO) and need to characterize the functionalities that are bond on the carbone lattice (of graphene). The main groups are :

- Hydroxyl
- Epoxy
- Carbonyls
- Carboxyls

I'm trying to develop a colorimetric method of quantification of the hydroxyls by selective derivatization. The problem is that I don't find any reaction that can be made selectively on a tertiary alcohol without reacting with the acids/carbonyls or the water present in the suspension of GO.

Has anyone any idea of a reagant that  :

- Can be measured by UV/VIS
- Reacts only with -OH groups (tertiary)
- Can be used in the presence of water

Any suggestion is appreciated :)

Thank you for reading

Offline pgk

  • Chemist
  • Full Member
  • *
  • Posts: 892
  • Mole Snacks: +97/-24
Re: Organic chemistry - specific derivatization of tertiary alcohol
« Reply #1 on: June 13, 2015, 01:32:12 PM »
A tertiary alcohol reacts rapidly, if it is shaken with concentrated hydrochloric acid at room temperature and forms a tertiary alkyl chloride. The so formed tertiary alkyl chloride, can further react with N,N-dialkyl aromatic diamine, without heating and leads to the corresponding quaternary ammonium salt, which can be measured by UV Spectroscopy.
R3C-OH  →  R3C-Cl  →  [R3CN(R2)Ar]+,Cl-
Please, note that quaternization of the N,N-dialkyl aromatic diamine, leads to auxochromy that helps the differentiation between the reagent and the derivative, by UV spectroscopy.
As an indicative reference: European Patent 0791575 (1997)
« Last Edit: June 13, 2015, 02:47:48 PM by pgk »

Offline Jall

  • Very New Member
  • *
  • Posts: 2
  • Mole Snacks: +0/-0
Re: Organic chemistry - specific derivatization of tertiary alcohol
« Reply #2 on: June 14, 2015, 01:01:27 PM »
Thank you very much for this insight.

I'm gonna try to makes the reaction on the graphite oxide lattice then filtrate the solid and analyse the filtrate by UV/VIS to see the quantity of reagant (probably N,N-dimethylaniline) that hasn't reacted.

Thank you again for your response

Sponsored Links