HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577273Generated: October 28, 2026
Ethyl Acetate → 2-(2-Bromoethoxy)ethyl 2-fluoro-3-morpholinobenzoate
https://huagongshe.com/reaction/577273
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Bis(2-bromoethyl) ether | HCID 21521 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3-Amino-2-fluorobenzoic acid | HCID 23094343 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-Bromoethoxy)ethyl 2-fluoro-3-morpholinobenzoate | HCID 66765171 | 38% |
Reaction Steps
To a solution of 3-amino-2-fluorobenzoic acid (500 mg, 3.1 mmol) in DMF (10 mL) was added DIEA (4.5 mL) and 2-bromoethylether (5 eq) and the reaction heated to 80° C. for 18 h. The reaction was allowed to cool to rt, diluted with EtOAc and washed with saturated NH4Cl (aq). The organic phase was dried (Na2SO4), filtered and concentrated in vacuo. The resultant residue was purified by column chromatography (petroleum ether: EtOAc) to give 2-(2-bromoethoxy)ethyl 2-fluoro-3-morpholinobenzoate (450 mg, 38%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040545B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-fed85b1e9e1c4d179e06d2de493b667b |
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| Source note | uspto-grants-2015_05 |
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