Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656317Generated: October 30, 2026

Phthalimide → HCID 22281061, compound

https://huagongshe.com/reaction/656317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantTetraethylene glycol p-toluenesulfonateHCID 13456094—
SolventDimethylformamideHCID 6228—
ProductHCID 22281061HCID 2228106180%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a stirred solution of 31.96 g (0.092 mol) of 2a in 400 mL of anhydrous DMF was added 14.2 g (1.05 equiv.) of phthalimide and 14.4 mL (1.05 equiv.) of 1,8-diazabicyclo[5.4.0]undec-7-ene. The solution was heated at 70° C. for 18 h then concentrated in vacuo. The crude yellow oil was purified by flash chromatography using 1600 mL of silica gel and eluting with 25% EtOAc-50% EtOAc-75% EtOAc in hexane, then EtOAc, then 10% MeOH-20% MeOH in EtOAc to afford 23.8 g (80%) of 3a as an oil. Upon standing, 3a became a waxy white solid. 1H NMR (300 MHz, CDCl3) d 7.84-7.78 (m, 2H), 7.70-7.66 (m, 2H), 3.86 (t, J=5.6 Hz, 2H), 3.70 (t, J=5.6 Hz, 2H), 3.64-3.51 (m, 12H), 2.67 (bs, 1H); 13C NMR (75 MHz, CDCl3) d 168.2, 133.8, 132.0, 123.1, 72.4, 70.5, 70.4, 70.2, 70.0, 67.8, 61.6, 37.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071737B2
Source datasetuspto-grants-2011_12
ORD IDord-89625b7ca015460081692e5b58c0a945
Source noteuspto-grants-2011_12