HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1832209Generated: October 27, 2026
Phthalimide → 2-[(1S)-3-Chloro-1-Phenylpropyl]-1H-Isoindole-1,3(2H)-Dione
https://huagongshe.com/reaction/1832209
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phthalimide | HCID 6809 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | (1R)-3-chloro-1-phenylpropan-1-ol | HCID 642409 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[(1S)-3-Chloro-1-Phenylpropyl]-1H-Isoindole-1,3(2H)-Dione | HCID 20722975 | 74% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07067534B1 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-9c14d69beea54f88b152742080d7f8fe |
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| Source note | uspto-grants-2006_06 |
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