HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507991Generated: October 25, 2026
Dimethylformamide → methyl 4-[(2-methyl-3,4-dihydroquinolin-1(2H)-yl)methyl]-3-[(methylsulfonyl)oxy]benzoate
https://huagongshe.com/reaction/507991
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methyl-1,2,3,4-tetrahydroquinoline | HCID 96289 | — |
| Reactant | Methyl 4-(bromomethyl)-3-[(methylsulfonyl)oxy]benzoate | HCID 23157330 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | methyl 4-[(2-methyl-3,4-dihydroquinolin-1(2H)-yl)methyl]-3-[(methylsulfonyl)oxy]benzoate | HCID 23157488 | 75% |
Reaction Steps
A mixture of methyl 4-(bromomethyl)-3-[(methylsulfonyl)oxy]benzoate (0.70 g, 2.2 mmol), 2-methyl-1,2,3,4-tetrahydroquinoline (0.39 g, 2.6 mmol), potassium carbonate (0.60 g, 4.3 mmol) and N,N-dimethylformamide (14 mL) was stirred at 70° C. for 23 hr. The reaction mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=10/1-2/1) to give the title compound (0.63 g, yield 75%) as a pale-yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07786165B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-6312856ef23848778fe07efbc22e69ae |
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| Source note | uspto-grants-2010_08 |
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