HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561329Generated: October 31, 2026
Phthalimide potassium salt → HCID 59656315, compound
https://huagongshe.com/reaction/561329
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Reactant | HCID 59656402 | HCID 59656402 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59656315 | HCID 59656315 | 36% |
Reaction Steps
To a solution of 4-bromomethyl-naphthalene-1-sulfonic acid cyclohexylamide 41 (150 mg, 0.39 mmol) in DMF (5 mL) was added potassium phthalimide (109 mg, 0.58 mmol). The resultant solution was stirred at room temperature and then heated to 100° C. for 3 hr. The reaction was quenched with water and extracted with CH2Cl2. The organic layers were dried and concentrated in vacuo. HPLC purification of the residue gave the title compound (G-4) (63 mg) as white foam. 1H NMR (300 MHz, MeOD) δ 8.67 (d, 1H), 8.42 (d, 1H), 8.22 (d, 1H), 7.88 (m, 23H), 7.76 (m, 4H), 5.48 (s, 2H), 4.48 (d, 1H), 3.12 (d, 1H), 1.58 (m, 6H), 1.10 (m, 4H); LC/MS m/z 449 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08063222B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-8fde3370bd394677888f5a09354671e8 |
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| Source note | uspto-grants-2011_11 |
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