HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889271Generated: October 29, 2026
Ethyl Acetate → Methyl 2-(2-benzyloxy-6-fluoroanilino)-acetate
https://huagongshe.com/reaction/889271
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | HCID 15219197 | HCID 15219197 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 2-(2-benzyloxy-6-fluoroanilino)-acetate | HCID 68430918 | — |
Reaction Steps
A mixture of 2-benzyloxy-6-fluoroaniline (950 mg, 4.37 mmol), methyl bromoacetate (456 μL, 737 mg, 4.82 mmol), and potassium carbonate (1.21 g, 8.76 mmols) in DMF (10 mL) is heated at 60° C. for 18 h. The mixture is poured into ethyl acetate and extracted once with water and five times with brine. The organic layer is dried, filtered, and the solvent removed under reduced pressure to afford a crude oil that is chromatographed on an Isco Companion (80 g silica gel, 0-30% gradient of hexane/ethyl acetate) to afford methyl 2-(2-benzyloxy-6-fluoroanilino)-acetate as an oil. MS (M+1)+=290; NMR (CDCl3): δ 7.39 (m, 5H), 6.67 (m, 3H), 5.10 (s, 2H), 4.57 (br s, 1H), 4.11 (m, 2H), 3.72 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08252820B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-84bc523a57de4e5baf62d1c7e360d8fe |
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| Source note | uspto-grants-2012_08 |
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