Benzene, (2-bromoethoxy)- → HCID 11569697, compound

HRID 1875608Notes

Reaction equation

HRID 1875608 reaction equation
[N:1]12[CH2:8][CH2:7][C:4]([C:9]([C:16]3[CH:20]=[CH:19][S:18][CH:17]=3)([C:11]3[CH:15]=[CH:14][S:13][CH:12]=3)[OH:10])([CH2:5][CH2:6]1)[CH2:3][CH2:2]2.[C:21]1([O:27][CH2:28][CH2:29][Br:30])[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>CO>[Br-:30].[OH:10][C:9]([C:11]1[CH:15]=[CH:14][S:13][CH:12]=1)([C:16]1[CH:20]=[CH:19][S:18][CH:17]=1)[C:4]12[CH2:7][CH2:8][N+:1]([CH2:29][CH2:28][O:27][C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)([CH2:6][CH2:5]1)[CH2:2][CH2:3]2

Participants

4

Reactant 2

HCID 68526Benzene, (2-bromoethoxy)-HCID 68963321HCID 68963321, compound

Product 1

HCID 11569697HCID 11569697, compoundYield 54.5%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

Following the general procedure outlined in Example 4, 1-azabicyclo[2.2.2]oct-4-yl(di-3-thienyl)methanol (0.0787 g, 0.258 mmol) and 2-bromoethyl phenyl ether (0.0839 g, 0.417 mmol) in 2 MeOH/3 CHCl3/2 CH3CN (5.0 mL) were reacted to give the desired product (0.0709 g, 54.5%). EI-MS m/z 426 (M+) Rt (1.85 min).

Workup

  1. customwere reacted

Sources & evidence

ORD record
ord-11d57a6da8da4bd5bc78369fa2beccb1
Source dataset
uspto-grants-2012_11
Patent number
US08309572B2

Reaction notes

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