Hexylamine → HCID 69503044, compound

HRID 1883395Notes

Reaction equation

HRID 1883395 reaction equation
P([O-])([O-])([O-])=O.[K+].[K+].[K+].CC1C=CC=C(C)C=1O.I[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=1[O:25][CH3:26].[CH2:27]([NH2:33])[CH2:28][CH2:29][CH2:30][CH2:31][CH3:32].CCCCCCCCCCCC>[Cu]I.O.C(OCC)C>[CH3:26][O:25][C:20]1[CH:21]=[CH:22][CH:23]=[CH:24][C:19]=1[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28][CH2:27][NH2:33]

Participants

9

Conditions

Temperature
80 °C

Procedure

Copper (I) iodide (10 mg, 0.05 mmol, 5 mol %), anhydrous fine powder potassium phosphate (425 mg, 2.0 mmol) and 2,6-dimethylphenol (24 mg, 0.2 mmol, 20 mol %) were put into a screw-capped test tube with a Teflon septum. The tube was evacuated and back-filled with argon (3 cycles). 2-Iodoanisole (130 μL, 1.0 mmol) and n-hexylamine (158 μL, 1.0 mmol) were added by micro-syringe at room temperature. The reaction mixture was heated at 80° C. for 18 hours. The reaction mixture was then allowed to reach room temperature. Diethyl ether (2 mL), water (2 mL) and dodecane (internal standard, 227 μL) were added. The organic layer was analyzed by GC to give 41% GC yield of N-(2-methoxyphenyl)hexylamine.

Workup

  1. customThe tube was evacuated
  2. additionback-filled with argon (3 cycles)
  3. customto reach room temperature

Sources & evidence

ORD record
ord-e4f395d48b214256b176481c151954f0
Source dataset
uspto-grants-2004_07
Patent number
US06759554B2

Reaction notes

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