HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1367129Generated: October 30, 2026
HCID 57974098, compound → Methyl 3,5-difluoro-α,α-dimethyl-δ-oxobenzenepentanoate
https://huagongshe.com/reaction/1367129
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 57974098 | HCID 57974098 | — |
| Reactant | HCID 178505930 | HCID 178505930 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 3,5-difluoro-α,α-dimethyl-δ-oxobenzenepentanoate | HCID 57974028 | — |
Reaction Steps
To a solution of methyl 5-[methoxy(methyl)amino]-2,2-dimethyl-5-oxopentanoate from Step C (4.68 g, 21.6 mmol) in THF (46.8 mL), cooled to 0° C., was added 3,5-difluorophenyl magnesium bromide (65 mL, 0.5 M in THF, 32.3 mmol) over 30 minutes. The reaction was allowed to stir at ambient temperature for 2 h, after which time no additional reaction progress was observed. Additional 3,5-difluorophenyl magnesium bromide (50 mL, 0.5 M in THF, 25.0 mmol) was added over 30 minutes. After 3 h at 0° C., the reaction was quenched by the rapid addition of a cold (0° C.) solution of EtOH (71 mL) and cone. HCl (5.0 mL). The reaction was then diluted with water (200 mL) and diethyl ether (400 mL). The organics were washed with water (200 mL×3) and brine (100 mL), then dried over sodium sulfate, filtered, and concentrated in vacuo to give a residue. This residue was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:hexanes—50:50 to 100:0, to give the title compound. MS: m/z=239 (M−31(MeO−)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893079B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-22ea8c5f65164cb8bc7651e0d2846b47 |
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| Source note | uspto-grants-2011_02 |
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