HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436123Generated: November 3, 2026
Ethyl Acetate → methyl(R)-2-tert-butoxycarbonylamino-6-(3,4-difluorophenyl)-6-oxohexanoate
https://huagongshe.com/reaction/1436123
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-(Tert-butyl) 2-methyl (R)-6-oxopiperidine-1,2-dicarboxylate | HCID 10729829 | — |
| Reactant | HCID 178505835 | HCID 178505835 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | methyl(R)-2-tert-butoxycarbonylamino-6-(3,4-difluorophenyl)-6-oxohexanoate | HCID 67461441 | — |
Reaction Steps
To a solution of (R)-6-oxopiperidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester (CAS No. 183890-36-0, 5.8 g) in THF (200 mL), 3,4-difluorophenylmagnesium bromide (0.5 M solution in THF, 50 mL) was added dropwise at −40° C., and the reaction solution was stirred at −40° C. for seven hours. A saturated ammonium chloride solution and ethyl acetate were added to the reaction solution, and the mixture was heated to room temperature. Thereafter, the organic layer was separated, and the resulting organic layer was dried over magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: heptane->heptane:ethyl acetate=1:1) to obtain 3.8 g of the title compound. The property value of the compound is as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07618960B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-b3d3a3412d374834a217a560784c503b |
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| Source note | uspto-grants-2009_11 |
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