HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2042646Generated: November 2, 2026
Ethyl bromoacetate → HCID 59652041, compound
https://huagongshe.com/reaction/2042646
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | HCID 59651884 | HCID 59651884 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59652041 | HCID 59652041 | 82% |
Reaction Steps
In a 250 mL round bottom flask, 4-(4-acetyl-3-fluoro-phenoxy)-piperidine-1-carboxylic acid tert-butyl ester (4.0 g, 12 mmol) in tetrahydrofuran (00 mL) were cooled to −78° C. Lithium diisopropylamide (1.4 g, 13 mmol) was added and stirred 30 min. then warmed to 0° C. Re-cooled to −78° C. and ethyl bromoacetate (1.4 mL, 13 mmol) in tetrahydrofuran (25 mL) was added. The reaction warmed to ambient temperature over 14 h. The reaction was quenched with NH4Cl sol. and the solvents were concentrated under vacuum. The reaction was chromatographed through silica gel with hexanes/ethyl acetate (7:3) as eluent to produce 4.10 g (82%) of oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08586588B2 |
|---|
| Source dataset | uspto-grants-2013_11 |
|---|
| ORD ID | ord-499e6d1abcae4657b9002c89efb1466d |
|---|
| Source note | uspto-grants-2013_11 |
|---|