HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747300Generated: November 1, 2026
1-Chloromethylnaphthalene → HCID 59497422, compound
https://huagongshe.com/reaction/1747300
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Chloromethylnaphthalene | HCID 6845 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 59497687 | HCID 59497687 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 59497422 | HCID 59497422 | 13% |
Reaction Steps
To a solution of 3-(6-Cyano-2-oxo-2,3-dihydro-benzimidazol-1-yl)-propionic acid ethyl ester (0.1 g, 0.39 mmol) in DMA (3 mL) were added 1-(chloromethyl)naphthalene (0.1 g, 0.58 mmol) and K2CO3 (0.11 g, 0.81 mmol). The reaction mixture was stirred at 65° C. for 16 h. When the reaction was complete, the reaction mixture was diluted with ethyl acetate and washed with water (×4). The organic phase was dried over Na2SO4 and concentrated. The resulting residue was purified by silica gel prep TLC using 98:2 CH2Cl2:MeOH as an eluent to afford 20 mg (13%) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150556B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-ce743809a1ed48fc87b037e112392ac8 |
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| Source note | uspto-grants-2015_10 |
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