1-Bromononane → HCID 11613146, compound

HRID 1817217Notes

Reaction equation

HRID 1817217 reaction equation
[N:1]12[CH2:8][CH2:7][C:4]([C:9]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)([C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)[C:10]#[N:11])([CH2:5][CH2:6]1)[CH2:3][CH2:2]2.[Br:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33]>>[Br-:24].[C:10]([C:9]([C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1)([C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1)[C:4]12[CH2:5][CH2:6][N+:1]([CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33])([CH2:2][CH2:3]1)[CH2:8][CH2:7]2)#[N:11]

Participants

3

Reactant 2

HCID 127421-BromononaneHCID 11716432HCID 11716432, compound

Product 1

HCID 11613146HCID 11613146, compoundYield 78.6%

Procedure

Following the general procedure outlined in Example 2, 1-azabicyclo[2.2.2]oct-4-yl(diphenyl)acetonitrile (0.0495 g, 0.164 mmol) and 1-bromononane (0.050 mL, 0.262 mmol) in 2CH3CN/3CHCl3 (4.0 mL) were reacted to give the desired product (0.0652 g, 78.6%). EI-MS m/z 429 (M+) Rt (2.55 min).

Workup

  1. customwere reacted

Sources & evidence

ORD record
ord-01e4ca849d144f9d9c6e32650ce04f71
Source dataset
uspto-grants-2009_10
Patent number
US07598267B2

Reaction notes

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