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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57974098HCID 57974098—
ReactantHCID 178505930HCID 178505930—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3,5-difluoro-α,α-dimethyl-δ-oxobenzenepentanoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893079B2
Source datasetuspto-grants-2011_02
ORD IDord-22ea8c5f65164cb8bc7651e0d2846b47
Source noteuspto-grants-2011_02