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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361062Generated: October 30, 2026

Hydroxylamine → (R)-6-(4-Fluoro-3-methylbenzyloxy)-2-(4-fluoro-3-methylphenoxy)-N-hydroxyhexanamide

https://huagongshe.com/reaction/1361062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
ReactantMethanolHCID 887—
ReactantPotassium CyanideHCID 9032—
Reactant(S)-3-((R)-6-(4-Fluoro-3-methylbenzyloxy)-2-(4-fluoro-3-methylphenoxy)hexanoyl)-4-isopropyloxazolidin-2-oneHCID 59775183—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(R)-6-(4-Fluoro-3-methylbenzyloxy)-2-(4-fluoro-3-methylphenoxy)-N-hydroxyhexanamideHCID 24991000—

Reaction Steps

To a solution of (S)-3-((R)-6-(4-fluoro-3-methylbenzyloxy)-2-(4-fluoro-3-methylphenoxy)hexanoyl)-4-isopropyloxazolidin-2-one (100 mg, 0.20 mmol) dissolved in 2 mL of THF, methanol, and 50 wt % NH2OH in H2O (2:2:1) was added KCN (4.0 mg, 0.06 mmol). The resulting mixture stirred for 3 days at room temperature. The reaction was quenched by the addition of 1M aqueous HCl (10 mL) and the resulting mixture extracted with ethyl acetate (3×10 mL). The combined organic layers were washed with brine (2×5 mL). The product was isolated by flash column chromatography eluting with 0% to 10% methanol/DCM to give the title compound (54.2 mg) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879911B2
Source datasetuspto-grants-2011_02
ORD IDord-3a31da602e3945f29029b08a105a5d14
Source noteuspto-grants-2011_02