Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412777Generated: October 30, 2026

4-Bromobenzophenone → [4-(Hexylamino)phenyl](phenyl)methanone

https://huagongshe.com/reaction/412777

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobenzophenoneHCID 7030—
ReactantHexylamineHCID 8102—
ReactantSodium t-butoxideHCID 23676156—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
SolventTolueneHCID 1140—
Product[4-(Hexylamino)phenyl](phenyl)methanoneHCID 6938734495.2%

Reaction Steps

According to the general procedure B, 4-Bromobenzophenone (131 mg, 0.50 mmol) reacted with n-hexylamine (52 mg, 0.52 mmol) using 1 mol % of Pd(dba)2, 2 mol % of Ph5FcP(t-Bu)2, and sodium tert-butoxide (58 mg, 0.60 mmol) in toluene at 50° C. for 13 h to give the title compound (134 mg, 93%) as a solid: 1H-NMR (300 MHz, CDCl3): δ 7.74, (t, 4H, J=8.4 Hz), 7.53-7.43 (m, 3H), 6.58 (d, 2H, J=8.7 Hz), 4.46 (bs, 1H), 3.17 (t, 2H, J=6.6 Hz), 1.61 (m, 2H), 1.42-1.32 (m, 6H), 0.91 (t, 3H, J=6.6 Hz). 13C{1H}-NMR (100 MHz, CDCl3): δ 195.00, 152.27, 139.11, 132.93, 131.00, 129.30, 127.89, 125.42, 111.02, 43.17, 31.44, 29.09. GC/MS(EI): m/z 281 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562989B2
Source datasetuspto-grants-2003_05
ORD IDord-6dd6441efdca4edf83ccde4f8576471e
Source noteuspto-grants-2003_05