HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892132Generated: October 29, 2026
Ethyl Acetate → Methyl 2-methyl-6-[3-(quinolin-2-ylmethoxy)-phenoxymethyl]-benzoate
https://huagongshe.com/reaction/892132
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 2-(bromomethyl)-6-methylbenzoate | HCID 10263795 | — |
| Reactant | Phenol, 3-(2-quinolinylmethoxy)- | HCID 10988736 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-methyl-6-[3-(quinolin-2-ylmethoxy)-phenoxymethyl]-benzoate | HCID 22241476 | — |
Reaction Steps
13-(Quinolin-2-ylmethoxy)-phenol (5.2 g, 21 mmol, example 3), methyl 2-bromomethyl-6-methyl-benzoate (example 2) (5.0 g, 21 mmol) and potassium carbonate (4.4 g, 32 mmol) are combined in DMF (50 mL) and heated at 85° C. for 3 h. The reaction is poured into ethyl acetate (500 mL) and washed with water (4×120 mL) and brine (100 mL). The solution is dried over magnesium sulfate, filtered and concentrated in vacuo to provide a residue which is purified by column chromatography (silica, 10 to 20% ethyl acetate in hexane) to provide the title compound. MS (ESI) 414 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07005440B1 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-cf1ccdfa8c5c4910b8291994e1d57646 |
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| Source note | uspto-grants-2006_02 |
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