HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485279Generated: October 30, 2026
3-(4-Cyanophenyl)propyl methanesulfonate → 4-(3-Phthalimidopropyl)benzonitrile
https://huagongshe.com/reaction/485279
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(4-Cyanophenyl)propyl methanesulfonate | HCID 21993646 | — |
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(3-Phthalimidopropyl)benzonitrile | HCID 13421303 | 85% |
Reaction Steps
To 100 ml of DMF suspension of 21.1 g (0.114 mol) of potassium phthalimide was added 50 ml of DMF solution of 13.6 g (57 mmols) of crude 4-(3-mesyloxypropyl)benzonitrile. The reaction mixture was stirred at 90° C. for 3 hours, then cooled to room temperature and poured into 200 ml of ice-water, followed by extraction with ether-benzene (1:1). The organic layer was dried over Na2SO4 and concentrated, giving 14.0 g (yield 85%) of 4-(3-phthalimidopropyl)benzonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04536391 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-263442db364047469babe0d857cfd484 |
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| Source note | uspto-grants-1985_08 |
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