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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403318Generated: November 3, 2026

Hydroxyamine hydrochloride → HCID 68325445, compound

https://huagongshe.com/reaction/2403318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
ReactantHCID 86671406HCID 86671406—
SolventMethanolHCID 887—
ProductHCID 68325445HCID 6832544584%

Reaction Steps

To a stirred solution of tert-butyl (RS)-2-(3-chloro-4-(diphenylmethyleneamino)phenyl)morpholine-4-carboxylate (0.63 g) in methanol (8 ml) were added sodium acetate (325 mg) and hydroxylamine hydrochloride (202 mg). The reaction mixture was stirred at room tempearture for 16 hours and then at 60° C. for 1 hour. The reaction mixture was then cooled to room temperature and concentrated in vacuo. The residue was purified by flash column chromatography (silica gel; gradient: 0% to 70% EtOAc in hexanes) to afford tert-butyl (RS)-2-(4-amino-3-chlorophenyl)morpholine-4-carboxylate (345 mg, 84%) as a white solid. MS (ISP): 337.2 ([{37Cl}M+Na]+), 335.1 ([{35Cl}M+Na]+), 314.9 ([{37Cl}M+H]+), 313.0 ([{35Cl}M+H]+), 259.1 ([{37Cl}M+H—C4H8]+), 257.1 ([{35Cl}M+H—C4H8]+), 215.3 ([{37Cl}M+H—C4H8—CO2]+), 213.0 ([{35Cl}M+H—C4H8—CO2]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802673B2
Source datasetuspto-grants-2014_08
ORD IDord-a8541b5f16344e2fb5ba0a11cec02f6d
Source noteuspto-grants-2014_08