Bwiti
(PVC-Analog Taste-Tester) 06-05-02 14:16 No 317819 |
Tosylate Salt Of 1-(1-Cyclohexenyl) Butylamine ? | Bookmark | ||||||
Goddamn fuckin' fuck. Alright, lets say 196g cyclohexanone and 146g n-butylamine was added to 600ml benzene, then it was distilled until all water had been removed. I want to convert this into a tosylate salt. This is done by adding p-toluenesulfonic acid monohydrate to toluene and distilling until all water is removed, and this is added to the 1-(1-cyclohexenyl) butylamine. What I'm dying to know is how much p-toluenesulfonic acid monohydrate do I add to the toluene? Any help would be much appreciated! Love my country, fear my government. |
||||||||
Osmium (Stoni's sexual toy) 06-05-02 14:53 No 317824 |
I think you should learn about moles and ... | Bookmark | ||||||
I think you should learn about moles and molecular weights and stuff. I'm not fat just horizontally disproportionate. |
||||||||
Bwiti (PVC-Analog Taste-Tester) 06-05-02 22:59 No 317940 |
Dammit! | Bookmark | ||||||
Dammit! I was hoping that no one would bring up my obvious weakness.. Alright, so is it as easy as reacting 1 mole of 1-(1-cyclohexenyl) butylamine with 1 mole p-toluenesulfonic acid? Then I react 1 mole phenyl-magnesium-iodide with 1 mole of the tosylate? I wish that my chemistry teacher in highschool wasn't such an uptight shit-fuck, then I wouldn't have to feel so retarded. Love my country, fear my government. |
||||||||
Rhodium (Chief Bee) 06-05-02 23:04 No 317942 |
But do you really want the imine tosylate (is ... | Bookmark | ||||||
But do you really want the imine tosylate (is that really stable)? You aren't trying to do a tosic acid catalyzed condensation of butylamine and cyclohexanone with azeotropic removal of the water in the dean-stark? But if you want to make a salt, yes - use one mole of each. |
||||||||
Bwiti (PVC-Analog Taste-Tester) 06-06-02 00:52 No 317982 |
Frustrated | Bookmark | ||||||
"But do you really want the imine tosylate" No, I'd rather smash my fingers with a hammer. My problem is that all patents that use a plain-old 1-(1-cyclohexenyl)amine (CHA) react it with phenyl-lithium. I want to use Mg, but I can't find one example that uses phenyl-magnesium on a CHA. In the patents, phenyl-Mg's always reacted with nitriles and in US3192219(example 1) it's reacted with the tosylate salt. Will phenyl-Mg work? If so, then why can't I find ANY examples? Love my country, fear my government. |
||||||||
Bwiti (PVC-Analog Taste-Tester) 06-07-02 06:08 No 318448 |
Any flat-out guesses? :-P | Bookmark | ||||||
Any flat-out guesses? Love my country, fear my government. |
||||||||
Osmium (Stoni's sexual toy) 06-07-02 11:27 No 318530 |
I don't understand what you're asking. | Bookmark | ||||||
I don't understand what you're asking. Have you seen this one already? ../rhodium /pcp/ena I'm not fat just horizontally disproportionate. |
||||||||
Bwiti (PVC-Analog Taste-Tester) 06-08-02 03:29 No 318727 |
Oops! I was getting confused between ... | Bookmark | ||||||
Oops! I was getting confused between imines/enamines.. Thanks, question answered. Love my country, fear my government. |
||||||||
Bwiti (PVC-Analog Taste-Tester) 06-08-02 16:25 No 318856 |
Btw | Bookmark | ||||||
Btw, would a little excess of anhydrous p-toluenesulfonic acid hinder the effectiveness of the phenyl-Mg-bromide? Love my country, fear my government. |
||||||||
Osmium (Stoni's sexual toy) 06-08-02 19:50 No 318899 |
Yes! | Bookmark | ||||||
Yes! I'm not fat just horizontally disproportionate. |
||||||||