Di(pentafluorophenyl)chloroethoxysilane → Ethoxy[tris(pentafluorophenyl)]silane

HRID 1829580Notes

Reaction equation

HRID 1829580 reaction equation
[F:1][C:2]1[C:7]([SiH:8]([C:13]2[C:18]([F:19])=[C:17]([F:20])[C:16]([F:21])=[C:15]([F:22])[C:14]=2[F:23])[O:9][CH2:10][CH2:11]Cl)=[C:6]([F:24])[C:5]([F:25])=[C:4]([F:26])[C:3]=1[F:27].[C:28]1([Li])[C:37]([F:38])=[C:35]([F:36])[C:33]([F:34])=[C:31]([F:32])[C:29]=1[F:30]>CCOCC>[F:38][C:37]1[C:28]([C:11]([C:13]2[C:14]([F:23])=[C:15]([F:22])[C:16]([F:21])=[C:17]([F:20])[C:18]=2[F:19])([C:28]2[C:37]([F:38])=[C:35]([F:36])[C:33]([F:34])=[C:31]([F:32])[C:29]=2[F:30])[CH2:10][O:9][SiH3:8])=[C:29]([F:30])[C:31]([F:32])=[C:33]([F:34])[C:35]=1[F:36].[Si:8]([O:9][CH2:10][CH3:11])([C:28]1[C:29]([F:30])=[C:31]([F:32])[C:33]([F:34])=[C:35]([F:36])[C:37]=1[F:38])([C:13]1[C:18]([F:19])=[C:17]([F:20])[C:16]([F:21])=[C:15]([F:22])[C:14]=1[F:23])[C:7]1[C:6]([F:24])=[C:5]([F:25])[C:4]([F:26])=[C:3]([F:27])[C:2]=1[F:1]

Participants

5

Reactant 2

HCID 131724616Di(pentafluorophenyl)chloroethoxysilaneHCID 178419089HCID 178419089, compound

Product 2

HCID 23523565Ethoxy[tris(pentafluorophenyl)]silaneHCID 131724617Tri(pentafluorophenyl)ethoxysilane

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent2×

Procedure

88.54 g (0.200 mol) of di(pentafluorophenyl)chloroethoxysilane in Et2O is slowly added to solution of C6F5—Li (0.200 mol, 34.80 g, prepared in situ) in Et2O at −78° C. The solution is stirred for over night allowing it to warm up to room temperature. Formed clear solution is filtered and evaporated to dryness to result tri(pentafluorophenyl)ethoxysilane, (C6F5)3SiOEt.

Workup

  1. customFormed clear solution
  2. filtrationis filtered
  3. customevaporated to dryness

Sources & evidence

ORD record
ord-53458f67a3054b53bedb4ea44ae2de57
Source dataset
uspto-grants-2006_06
Patent number
US07062145B2

Reaction notes

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