Cyclohexyl bromide → HCID 86733495, compound

HRID 1657329Notes

Reaction equation

HRID 1657329 reaction equation
C1([Br:7])CCCCC1.[Br-].[CH:9]1([N+:15]([CH3:28])([CH3:27])[CH:16]2[CH2:21][CH:20]([CH:22]([CH3:24])[CH3:23])[CH2:19][CH2:18][C:17]2([OH:26])[CH3:25])[CH2:14][CH2:13]C[CH2:11][CH2:10]1>>[Br-:7].[CH:9]1([N+:15]([CH3:28])([CH3:27])[CH:16]2[CH2:21][CH:20]([CH:22]([CH3:24])[CH3:23])[CH2:19][CH2:18][C:17]2([OH:26])[CH3:25])[CH2:14][CH2:13][CH2:11][CH2:10]1

Participants

3

Reactant 2

HCID 7960Cyclohexyl bromideHCID 86733496HCID 86733496, compound

Product 1

HCID 86733495HCID 86733495, compound

Procedure

By analogues procedure using cyclohexyl bromide there was also prepared cyclohexyl dimethyl (1-hydroxy-p-menth-2-yl) ammonium bromide.

Sources & evidence

ORD record
ord-f7c9216019264a42a1e8545989c7fe39
Source dataset
uspto-grants-1976_06
Patent number
US03960539

Reaction notes

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