pickle11
(Stranger) 11-26-02 04:28 No 383362 |
oihkal? | Bookmark | ||||||
correct me if im wrong. 1. tartaric acid can be isolated from cream of tartar. 2. tartaric acid can be reduced to succinic acid using I/H2S. 3. succinic acid can be neutralized with ammonium hydroxide and heated to form succinamide. 4. succinamide can be reacted ala ../rhodium /nbs.htm 5. n-bromosuccinamide can be used ala ../rhodium /ppa.syn 6. phenylpropanolamines can be reacted with cyanogen bromide to yield various ring substituted methylaminorex analogs. oxazolines i have known and loved. I dont think any of them would be controlled substances or classified as analogs. |
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Rhodium (Chief Bee) 11-26-02 05:28 No 383371 |
Yes, technically. But if you don't want to buy ... | Bookmark | ||||||
Yes, technically. But if you don't want to buy NBS, then please buy succinimide or at least succinic anhydride - those two are not watched the least. Aqueous bromine also does the same job as NBS, but not as cleanly (= lower yield). But a whole lot less work than your proposition, I promise. Also, it is much easier to make aminorex analogs from PPAs using potassium cyanate than with cyanogen bromide - the former is non-toxic, the latter is a vile volatile poison. |
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pickle11 (Stranger) 11-26-02 05:48 No 383379 |
bromohydrine? | Bookmark | ||||||
what about the bromohydrine in the ppa synth. is that repaceable, available, easily synthesized? |
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Rhodium (Chief Bee) 11-26-02 05:54 No 383382 |
As I said, you can make that with aqueous bromine ... | Bookmark | ||||||
As I said, you can make that with aqueous bromine instead of NBS - UTFSE here or at http://patft.uspto.gov/netahtml/search-b |
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L42L (Stranger) 12-04-02 00:22 No 385930 |
Could you elaborate? | Bookmark | ||||||
I'm afraid I need more info. Searched a few key words (or so i thought ) into TFSE and am at a loss. Asarone-ppa ala aq Br !?! Any sugestions/hints/info/direction from any bee concerning this would be fab. thanks, lurk |
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Rhodium (Chief Bee) 12-04-02 11:30 No 386135 |
Search for "bromohydrin". | Bookmark | ||||||
Search for "bromohydrin". Compounds with adjacent OH and Br groups are called that. Then you just select one of the preparations you find which doesn't use NBS. |
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L42L (Stranger) 01-17-03 19:56 No 399101 |
help with succinic acid to succinamide | Bookmark | ||||||
Could some bee help with a theoretical procedure for this. Ammonium hydroxide and heat? The idea of synthing a new compound (even if it is a questionable aminorex) is thrilling to say the least. Thanks for the spark pickle11. Thanks beez, Lurk BTW Rhodium: It aint much but its more than nothing. Its in the mail this weekend ($) Your efforts are truly priceless. Thanks! |
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SPISSHAK (Hive Addict) 01-17-03 20:16 No 399104 |
I like that concept | Bookmark | ||||||
oxazolamines I have known and loved sounds like an intersting sequel to the phenylethylamines, too bad no one has done any research on the pharmacology or chemistry of ring substituded phenyloxazolamines. |
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starlight (Hive Bee) 01-18-03 12:34 No 399368 |
just be aware of this | Bookmark | ||||||
Post 346726 (Dr_Heckyll: "4-Methylaminorex Dangers", General Discourse) |
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