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Butyl iodide → alpha-Ionene

HRID 1648838
Notes
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Reaction equation

HRID 1648838 reaction equation
I[CH2:2][CH2:3][CH3:4].I[CH2:6]CCCCC.ICCCCCCCCCCCC.ICCCC.BrC(Br)=CCC.I[C:37](I)([CH3:39])[CH3:38].IC(I)C.Br[C:46]1[C:47](Br)=[C:48]([CH3:53])[CH:49]=[CH:50]C=1C>>[CH3:4][C:3]1[CH:2]=[CH:50][C:49]2[C:48]([CH3:53])([CH3:6])[CH2:47][CH2:46][CH2:39][C:37]=2[CH:38]=1
ParticipantsProcedureSources & evidenceReaction notes

Participants

9

Reactant 8

HCID 10962Butyl iodideHCID 125271-IodohexaneHCID 202821-IodododecaneHCID 336431-IodopropaneHCID 68980DiiodoethaneHCID 11483316Propane, 2,2-diiodo-HCID 12554946HCID 12554946, compoundHCID 226384832,3-Dibromo-1,4-dimethylbenzene

Procedure

A series of ionene polymers were prepared according to the procedure of Example 1 except that equivalent amounts of iodo-propane, iodo-hexane, iodo-dodecane, iodo-butane or a mixture of dibromobutene and diiodopropane or diiodoethane were substituted for dibromo-p-xylene.

Sources & evidence

ORD record
ord-835e17f68a3142999e1e3fc1c979733c
Source dataset
uspto-grants-1983_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US04414080

Reaction notes

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On this pageParticipantsProcedureSources & evidenceReaction notes

Product 1

HCID 68057alpha-Ionene