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

HRID 1803682Notes

Reaction equation

HRID 1803682 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-6111c26861a240869ff898ba5b88e34d
Source dataset
uspto-grants-2013_01
Patent number
US08349869B2

Reaction notes

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