Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
  • C07F17/00—Metallocenes
  • C07F17/02—Metallocenes of metals of Groups 8, 9 or 10 of the Periodic Table
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
  • C07B53/00—Asymmetric syntheses
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C1/00—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon
  • C07C1/32—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from compounds containing hetero-atoms other than or in addition to oxygen or halogen
  • C07C1/325—Preparation of hydrocarbons from one or more compounds, none of them being a hydrocarbon starting from compounds containing hetero-atoms other than or in addition to oxygen or halogen the hetero-atom being a metal atom
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C17/00—Preparation of halogenated hydrocarbons
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
  • C07C41/01—Preparation of ethers
  • C07C41/18—Preparation of ethers by reactions not forming ether-oxygen bonds
  • C07C41/30—Preparation of ethers by reactions not forming ether-oxygen bonds by increasing the number of carbon atoms, e.g. by oligomerisation
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C67/00—Preparation of carboxylic acid esters
  • C07C67/28—Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group
  • C07C67/293—Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
  • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
  • C07B2200/07—Optical isomers

Definitions

• This invention relates to selective synthesis and catalysts therefor.
• an allylic compound is reacted with an organozinc compound Zn(R 6 ) 2 to eliminate a group (the leaving group) from the allylic compound and to add a group from the organozinc compound to it in the presence of a copper salt catalyst and a chiral organic ligand for the copper.
• the ligand is a primary or secondary amine in which the nitrogen atom is directly linked to the chiral centre.
• the allylic compound is suitably of formula t
• X is the leaving group for example a chlorine atom and in which A is hydrogen or an alkyl or aryl group, preferably having 0-20 carbon atoms. If substitution occurs at the carbon atom marked * a chiral centre may be formed. This process is known as Sn2'substitution; an alternative substitution at the carbon atom marked
• the reactions are shown as follows:
• R 6 is a group from the organozinc compound.
• the former reaction is generally favoured and is influenced by the leaving group, ligands and solvents as shown below, tetrahydofuran being a particularly favourable solvent.
• the process is normally chemoselective for Sn2' substitution and/or stereoselective.
• the reaction is as shown below:-
• R 1 - R 6 are alkyl, alkenyl, alkynyl, aryl, aralkyl or heterocyclyl groups optionally substituted by for example halogen, alkoxy, aryloxy, acytoxy, nitro, amide, acetamide, carboxylate, cyano, acetal, sulphide, sulphonate, sulfone, sulfoxide, phosphite, phosphonate, phosphine groups, each preferably having at most 20 and preferably less than 10 carbon atoms, or R 1 to R 5 may be H, R 7 is an aryl for example a phenyl or ferrocenyl or substituted aryl or ferrocenyl group of which the substituents may be for example 1- aminobenzyl, 1-amino-2-naphthylmethyl, 1-amino-(4-tert-butylphenyl)methyl, trimethylsilyl, phosphite
• X is halogen, OR 9 , OCOR 9 , OCO 2 R 9 , OSO 2 R 9 , OCS 2 R 9 CH(OR 10 ) 2 , OPO (OR 9 ) 2 , SOR 9 , or SO 2 R 9 where R 9 and R 10 are optionally substituted C C ⁇ 0 alkyl or aryl, of which the substituents may be halogen, nitro, methoxy, trifluoromethoxy, methyl, ethyl, tert butyl or sulphonate groups 0 e.g.
• R7 and R8 may together form a 5 or 6 membered carbocyclic or heterocyclic ring providing that a carbon atom to which the nitrogen is attached is chiral.
• R7 and R8 together may be 1-indane, bornylamine or 2-cyclohexylamine.
• Y is halogen, carboxylate for example, acetate, acetoacetate, cyanide, or thiocyanate and 5 Z is an ether or thioether for example dimethylsulfide, tetrahydrofuran or diethylether.
• R 1 - R 2 and R 3 and one of R 4 or R 5 are H and the other one of R 4 or R 5 is aryl, for example phenyl, 4-chlorophenyl or 4-trifluoromethyl phenyl or is a trialkyl (e.g. tri- isopropyl) silyl oxymethyl groups
• R 6 is alkyl, tri-alkyl (e.g. trimethyl) silyl methyl, phenyl or 2,2-dimethylbut-3-enyl.
• R 7 is ferrocenyl
• R 8 is naphthyl
• X is chloride
• Y chloride or o bromide
• Z dimethylsulfide.
• R 5 is preferably phenyl and R 6 is preferably neopentyl.
• the substituents of R 7 preferably have at most 10 carbon atoms in total and those of R 8 preferably at most 8 carbon atoms in total.
• Alkanes, cyclo alkanes and/or aromatic solvents for example toluene may be present.
• Preferred solvents are ethers for example diethylether, 1 ,4-dioxane, 5 tertbutylmethylether and especially tetrahydrofuran.
• Preferred temperatures are -120°C to 25°C more preferably -100°C to 20°C and especially -90°C to -50°C.
• Preferred concentrations of catalyst are 0.1 atom% to 20 atom%, especially 0.5 atom% to 5 atom% expressed as copper atoms based on moles of the allylic compound. o
• the ratio of copper atoms to the amine ligand molecules is suitably 1 : 10 to 2: 1.
• A is a ferrocenyl or substituted ferrocenyl group and B is a group R 8 other than a methyl or phenyl group are believed to be novel.
• the groups A and B should be 5 different in order to obtain stereospecificity.
• B is preferably a 2-naphthyl group .
• the catalyst is prepared from 1 ,1-diphenyl pyrrolidine methanol and borane (see Synlett).
• the ferrocenyl alcohol (4.0 g, 11.6 mmol) was dissolved in dry pyridine (30 ml) and acetic anhydride (20 ml) at room temperature. After stirring for 18h at room temperature all volatiles were removed under high vacuum at 50°C furnishing the pure acetylated alcohol (4.5 g, 100 %) as a red glue, that smoothly crystallised on standing to a red solid.
• acetylated alcohol (3.0 g, 8 mmol) was dissolved in acetonitrile (200 ml) and
• Table 1 shows the use of different chiral organic ligands (lig * ) R 7 and R 8 as indicated in table 1 , in the reaction of cinnamyl chloride with di-neopentyl zinc at -50°C.
• the chiral organic ligands were prepared according to the methods in example 1 and are of the (R) configuration. The experimental conditions are analogous to those in Example 2 above. Table 1
• the experimental conditions are analogous to those in Example 2 above. Table 4

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Catalysts (AREA)
• Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
• Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)

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• 1998
  • 1998-08-28 GB GBGB9818701.6A patent/GB9818701D0/en not_active Ceased
• 1999
  • 1999-08-25 JP JP2000567486A patent/JP2002523479A/ja not_active Withdrawn
  • 1999-08-25 AT AT99940407T patent/ATE265405T1/de not_active IP Right Cessation
  • 1999-08-25 US US09/763,963 patent/US6610871B1/en not_active Expired - Fee Related
  • 1999-08-25 EP EP99940407A patent/EP1107936B1/en not_active Expired - Lifetime
  • 1999-08-25 AU AU54386/99A patent/AU5438699A/en not_active Abandoned
  • 1999-08-25 DE DE69916857T patent/DE69916857T2/de not_active Expired - Fee Related
  • 1999-08-25 WO PCT/GB1999/002807 patent/WO2000012449A1/en not_active Ceased
  • 1999-08-25 CA CA002341860A patent/CA2341860C/en not_active Expired - Fee Related

Non-Patent Citations (4)

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