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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412776Generated: October 29, 2026

Hexylamine → HCID 9813085, compound

https://huagongshe.com/reaction/412776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexylamineHCID 8102—
Reactant4-ChlorobenzonitrileHCID 12163—
ReactantPotassium Phosphate, TribasicHCID 62657—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 9813085HCID 981308591.9%

Reaction Steps

According to the general procedure B, 4-Chlorobenzonitrile (69 mg, 0.50 mmol) reacted with n-hexylamine (80 μl, 0.60 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 70° C. for 8 h to give the title compound as a solid (79 mg, 78%). On the other hand, the reaction of 4-chlorobenzonitrile (69 mg, 0.50 mmol) with n-hexylamine (61 mg, 0.60) using K3PO4 and DME also occurred in 92% yield to afford the title compound (93 mg) at 100° C. for 13 h. 1H-NMR (300 MHz, CDCl3): δ 7.39 (d, 2H, J=8.4 Hz), 6.54 (d, 2H, J=8.7 Hz), 4.34 (bs, 1H, —NH—), 3.13 (t, 2H, J=6.9 and 7.2 Hz). 13C{1H}-NMR (100 MHz, CDCl3): δ 151.43, 133.47, 120.60, 111.56, 97.69, 43.03, 31.37, 28.89, 26.55, 22.43, 13.88. GC/MS(EI): m/z 202 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06562989B2
Source datasetuspto-grants-2003_05
ORD IDord-eb0de5ce698b491cab76ef4933e8a057
Source noteuspto-grants-2003_05