7-Bromo-1-heptene → N-(hept-6-enyl)phthalimide

HRID 579631Notes

Reaction equation

HRID 579631 reaction equation
[C:1]1(=[O:11])[NH:5][C:4](=[O:6])[C:3]2=[CH:7][CH:8]=[CH:9][CH:10]=[C:2]12.[K].Br[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH:19]=[CH2:20]>CN(C=O)C>[CH2:20]([N:5]1[C:1](=[O:11])[C:2]2=[CH:10][CH:9]=[CH:8][CH:7]=[C:3]2[C:4]1=[O:6])[CH2:19][CH2:18][CH2:17][CH2:16][CH:15]=[CH2:14]

Participants

4

Reactant 2

HCID 5244507-Bromo-1-hepteneHCID 24194345Phthalimide potassium salt

Product 1

HCID 53236045N-(hept-6-enyl)phthalimide

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

A solution of potassium phthalimide (627 mg, 3.38 mmol) and 7-bromohept-1-ene in dry DMF (10 mL) was stirred at 100° C. under nitrogen for 1 h. Then, the reaction mixture was successively cooled to room temperature, filtered, diluted with ether, and filtered again. The filtrate was concentrated under reduced pressure to give the target product 75 as an oil, which was used without further purifications in the next step: m/z=244 (M+H)+.

Workup

  1. filtrationfiltered
  2. additiondiluted with ether
  3. filtrationfiltered again
  4. concentrationThe filtrate was concentrated under reduced pressure

Sources & evidence

ORD record
ord-2f149da2a50348a0997199a69a5b0690
Source dataset
uspto-grants-2015_05
Patent number
US09040562B2

Reaction notes

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