HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355673Generated: October 30, 2026
4-(Chloromethyl)pyridinium chloride → HCID 18507782, compound
https://huagongshe.com/reaction/1355673
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(Chloromethyl)pyridinium chloride | HCID 74570 | — |
| Reactant | HCID 18507786 | HCID 18507786 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18507782 | HCID 18507782 | — |
Reaction Steps
To a solution of 6-bromo-7-methyl-1-naphthalen-2-ylmethyl-1,3-dihydro-indol-2-one (495.7 mg, 1.36 mmol) in THF (30 ml) was added 4-picolyl chloride hydrochloride (893 mg, 5.45 mmol). The resulting suspension was purged with nitrogen gas for 10 minutes, after which time an aqueous potassium hydroxide (1N, 10.88 ml, degassed for 10 minutes prior to the addition) was added dropwise at room temperature. The dark solution was stirred at room temperature overnight. After removal of THF, the reaction mixture was partitioned between water and ethyl ether. The organic layer was dried over MgSO4, filtered and concentrated under vacuum to give the crude product. It was chromatographed on flash silica gel eluting with ethyl acetate to provide the title compound of 2D (524 mg, 0.956 mmol, 70.3% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06586447B1 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-c9a3eac64cdd4824ad478e76cbcd68b1 |
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| Source note | uspto-grants-2003_07 |
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