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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273435Generated: October 30, 2026

4-Methylmorpholine → HCID 72575117, compound

https://huagongshe.com/reaction/273435

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 69205989HCID 69205989—
SolventDimethylformamideHCID 6228—
SolventChloroform methanolHCID 21584188—
ProductHCID 72575117HCID 7257511746%

Reaction Conditions

Temperature0 °C

Reaction Steps

Acid compound 11 (1.9 g, 4.43 mmol) was dissolved in N,N-dimethylformamide (20 mL) and stirred under an atmosphere of argon. N-Methylmorpholine (1.95 mL, 18.0 mmol) was added, the reaction mixture was cooled to 0° C. and BOP reagent (2.16 g, 4.88 mmol) was added. After 20 min, hydroxylamine hydrochloride (0.62 g, 8.87 mmol) was added and the reaction mixture was warmed up to room temperature and stirred overnight. The solvent was removed under reduced pressure and residual material was partitioned between EtOAc (50 mL) and saturated NH4Cl solution (1×30 mL). The organic layer was dried and concentrated to yield the crude material. Flash chromatography over silica gel using chloroform-methanol (19:1) yielded the desired hydroxamic acid compound 12 (0.9 g, 46%). 1H NMR (DMSO-d6): 8.95 (br, 1H), 7.73 (d, J=9.2 Hz, 2H), 7.28 (d, J=8.4 Hz, 2H), 7.18 (d, J=8.4 Hz, 1H), 7.00 (d, J=8.8 Hz, 2H), 6.95 (d, J=8.8 Hz, 2H), 4.55 (m, 1H), 2.91 (s, 3H), 2.70-2.90 (m, 5H), 1.30 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456292B2
Source datasetuspto-grants-2008_11
ORD IDord-6bda4c9177e247f39f34f330999d3500
Source noteuspto-grants-2008_11