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2. chem.libretexts.org › Bookshelves › Organic_Chemistry24.6: Synthesis of Amines - Chemistry LibreTexts

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   Alkylation is an efficient method for the synthesis of 3 o and 4 o amines. However, when 1 o and 2 o amines are alkylated a mixture of products is typically produced. When ammonia is reacted with an alkylhalide an monoalkylammonium salt is formed. RX + NH 3 → RNH 3+ + X -.

3. www.ocr.org.uk › Images › 359182-organic-synthesisSynthetic routes (A Level) reaction pathways Aliphatic compounds

   www.ocr.org.uk › Images › 359182-organic-synthesis

   OCR, A Level, Chemistry A, Topic Exploration Pack, Reaction pathways Created Date: 20170207082346Z ...

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4. People also ask

   What are some examples of psychoactive arylcycloalkylamines?

   • Classic examples of psychoactive arylcycloalkylamines include ketamine and 1- (1-phenylcyclohexyl)piperidine (PCP) and many others serve as important structural templates for neuropharmacological research.

   Preparation and analytical characterization of 1‐(1‐phenylcyclohexyl

   analyticalsciencejournals.onlinelibrary.wiley.com/doi/10.1002/dta.1468

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   How many substituted 1 phenylcyclohexyl pyrrolidine analogues are there?

   • The present study describes the synthesis of three substituted 1- (1-phenylcyclohexyl)piperidines, (3-MeO-, 4-MeO- and 3-Me-PCP) and three substituted 1- (1-phenylcyclohexyl)pyrrolidine analogues (3-MeO-, 4-MeO- and 3-Me-PCPy).

   Preparation and analytical characterization of 1‐(1‐phenylcyclohexyl

   analyticalsciencejournals.onlinelibrary.wiley.com/doi/10.1002/dta.1468

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   How are arylamines prepared?

   • Arylamines are typically prepared by the reduction of a nitro group on an aromatic ring. Several methods for reducing nitro groups to amines are known. These include catalytic hydrogenation (H 2 + platinum catalyst), and zinc, iron, or tin (II) chloride in dilute mineral acid. The procedures described above are sufficient for most cases.

   24.6: Synthesis of Amines - Chemistry LibreTexts

   chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/24:_Amines_and_Heterocycles/24.06:_Synthesis_of_Amines

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   Which pathway provides the simplest amine starting material?

   • Because the amine is commonly used in excess during a reductive animation, the pathway which provides the simplest amine starting material is preferred. The carbon from the broken C-N bond goes on to become a carbonyl starting material. The nitrogen gains a hydrogen to become the amine starting material.

   24.6: Synthesis of Amines - Chemistry LibreTexts

   chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/24:_Amines_and_Heterocycles/24.06:_Synthesis_of_Amines

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5. webbook.nist.gov › cgi › cbookN-Phenylcyclohexylamine - NIST Chemistry WebBook

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   Feb 6, 2010 · IUPAC Standard InChI: InChI=1S/C12H17N/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1,3-4,7-8,12-13H,2,5-6,9-10H2 Copy IUPAC Standard InChIKey: TXTHKGMZDDTZFD-UHFFFAOYSA-N ...

6. www.erowid.org › archive › rhodiumThe Synthesis of Phencyclidine and Other 1 ... - Erowid

   www.erowid.org › archive › rhodium

   thesis of 1-phenylcyclohexylamine. The compound prepared by the alternate route (method F) was identi- cal in all respects with the one obtained prepared from Method F aC6"I NCO - CxCeH5 "2 VI phenylcyclohexene. Recently, Cristol, et ul., re- ported the isolation of the amine as its benzoyl deriva- tive via a modified Ritter reaction.

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7. webbook.nist.gov › cgi › cbookN-Phenylcyclohexylamine - NIST Chemistry WebBook

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   Feb 6, 2010 · All mass spectra in this site (plus many more) are available from the NIST/EPA/NIH Mass Spectral Library. Please see the following for information about the library and its accompanying search program.

8. analyticalsciencejournals.onlinelibrary.wiley.comPreparation and analytical characterization of 1‐(1 ...

   analyticalsciencejournals.onlinelibrary.wiley.com

   Apr 2, 2013 · Drug Testing and Analysis is a specialist journal covering sports doping, recreational drugs, pharmaceuticals, toxico-pathology, forensics, and the environment.

9. chemistry.mdma.ch › hiveboard › rhodiumUse of PCA (1-phenylcyclohexylamine) as a precursor

   chemistry.mdma.ch › hiveboard › rhodium

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   An attractive procedure from the standpoint of clandestine synthesis would be the reductive alkylation of PCA with acetone and aluminum amalgam to give the potent analog N-isopropyl phenylcyclohexylamine. The first method using PCA as an intermediate is Scheme IV. This route has received little attention among clandestine chemists, but has ...