Jump to content
Science Forums

Diamporphine hydrochloride and derivatives


joho

Recommended Posts

ACUTALLY:

I want to change my above answer. :)

My mistake.... I am fairly certain that it WOULD produce the free base form by reacting it with sodium hydroxide.

Sorry.....:)

 

Thanks, but can you give me an idea how? An equation maybe or point me somewhere I can find one?

Link to comment
Share on other sites

An amine hydrochloride will obviously be neutralized by sodium hydroxide solution. Look at the pKa values. Kinetics of reaction can depend on steric hindrance and electronics, e.g., 2,2,6,6-tetramethylpiperidine and 1,8-bis(dimethylamino)naphthlene.

 

Will NaOH do evil to other parts of your molecule?

Link to comment
Share on other sites

An amine hydrochloride will obviously be neutralized by sodium hydroxide solution. Look at the pKa values. Kinetics of reaction can depend on steric hindrance and electronics, e.g., 2,2,6,6-tetramethylpiperidine and 1,8-bis(dimethylamino)naphthlene.

 

Will NaOH do evil to other parts of your molecule?

 

Mmmhhm. Yep. Yep. I see. Thanks. Haven't got a clue what you mean but thanks! Like the pic - hope thats not you!::)

Link to comment
Share on other sites

Mmmhhm. Yep. Yep. I see. Thanks. Haven't got a clue what you mean but thanks! Like the pic - hope thats not you!::hihi:

 

I find that if you re-read old UncleAl's posts about 3-2,000 times they actually start to make sense.

 

At least I see I am not alone.

Link to comment
Share on other sites

Join the conversation

You can post now and register later. If you have an account, sign in now to post with your account.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...