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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2087202Generated: October 27, 2026

Phthalimide → 2-[(1S)-3-Chloro-1-Phenylpropyl]-1H-Isoindole-1,3(2H)-Dione

https://huagongshe.com/reaction/2087202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant(1R)-3-chloro-1-phenylpropan-1-olHCID 642409—
SolventTetrahydrofuranHCID 8028—
Product2-[(1S)-3-Chloro-1-Phenylpropyl]-1H-Isoindole-1,3(2H)-DioneHCID 2072297574%

Reaction Steps

Triphenylphosphine (5.25 g, 20.0 mmol) and diethyl azodicarboxylate (3.58 g, 20.0 mmol) were added to a solution of (1R)-3-chloro-1-phenyl-1-propanol (3.42 g, 20.0 mmol) and phthalimide (2.94 g, 20.0 mmol) in THF (100 mL). The reaction mixture was stirred for 4 h at room temperature. The solvent was removed under reduced pressure and the residue was triturated with pentane (3×50 mL). The combined pentane fractions were concentrated in vacuo and the crude product was purified by chromatography on silica using EtOAc/hexane (3:97) to give the desired product (4.40 g, 74%). 1H NMR (400 MHz, CDCl3) δ 7.82 (d, 1H, J=5.7 Hz), 7.81 (d, 1H, J=5.5 Hz), 7.70 (d, 1H, J=5.4 Hz), 7.69 (d, 1H, J=5.8 Hz), 7.55 (d, 2H, J=7.2 Hz), 7.38-7.28 (m, 3H), 5.64 (dd, 1H, J=6.8, 9.2 Hz), 3.56 (t, 2H, J=6.4 Hz), 3.11-3.02 (m, 1H) 2.85-2.75 (m, 1H); ESMS m/e: 300.1 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06727264B1
Source datasetuspto-grants-2004_04
ORD IDord-9ff67a5285ca4cb7ba1e818551154371
Source noteuspto-grants-2004_04