Sciencemadness Discussion Board
Not logged in [Login ]
Go To Bottom

Printable Version  
Author: Subject: Hydroiodic acid and sodium ethoxide/butoxide sources
argox120
Harmless
*




Posts: 20
Registered: 3-1-2022
Member Is Offline


[*] posted on 4-10-2024 at 10:48
Hydroiodic acid and sodium ethoxide/butoxide sources


would like to get my hands on these reagents"
Hydroiodic acid(250-500ml) and sodium ethoxide or sodium tertbutoxide(100g-250g) for a reduction of teriary alcohol.
View user's profile View All Posts By User
Sir_Gawain
Hazard to Others
***




Posts: 402
Registered: 12-10-2022
Location: Due South of Due West
Member Is Offline

Mood: Like a pendulum

[*] posted on 4-10-2024 at 17:58


Are you unable to make them yourself? That’s likely going to be easier than buying.



“Alchemy is trying to turn things yellow; chemistry is trying to avoid things turning yellow.” -Tom deP.
View user's profile Visit user's homepage View All Posts By User
j_sum1
Administrator
********




Posts: 6307
Registered: 4-10-2014
Location: At home
Member Is Online

Mood: Most of the ducks are in a row

[*] posted on 4-10-2024 at 22:48


Duplicate thread. I am closing the other one.
View user's profile View All Posts By User
bnull
Hazard to Others
***




Posts: 386
Registered: 15-1-2024
Location: South of the border, wherever the border is.
Member Is Offline

Mood: Dazed and confused.

[*] posted on 5-10-2024 at 05:38


There are other routes available that don't make use of HI or EtONa. What tertiary alcohol is it?



Quod scripsi, scripsi.

B. N. Ull

P.S.: Did you know that we have a Library?
View user's profile View All Posts By User
argox120
Harmless
*




Posts: 20
Registered: 3-1-2022
Member Is Offline


[*] posted on 5-10-2024 at 08:42


it is a benzylic tertiary alchol like 1,1 dimethyl benzyl alcohol
View user's profile View All Posts By User
bnull
Hazard to Others
***




Posts: 386
Registered: 15-1-2024
Location: South of the border, wherever the border is.
Member Is Offline

Mood: Dazed and confused.

[*] posted on 5-10-2024 at 12:34


2-phenyl‐2-propanol, eh? Trying to make cumene and analogues?

What about generating HI in situ?

I remember seeing something for tertiary alcohols, like a Wolff-Kischner. Are you following a published procedure?

I ask those questions because there're probably other ways that don't need HI or EtONa.




Quod scripsi, scripsi.

B. N. Ull

P.S.: Did you know that we have a Library?
View user's profile View All Posts By User
Random
International Hazard
*****




Posts: 1120
Registered: 7-5-2010
Location: In ur closet
Member Is Offline

Mood: Energetic

[*] posted on 5-10-2024 at 12:51


Does it need to be Sodium Ethoxide or can Magnesium Ethoxide be used?
View user's profile View All Posts By User

  Go To Top