Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096589Generated: October 30, 2026

N-methylhydroxylamine hydrochloride → HCID 58423904, compound

https://huagongshe.com/reaction/2096589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methylhydroxylamine hydrochlorideHCID 77906—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 178511906HCID 178511906—
SolventMethanolHCID 887—
ProductHCID 58423904HCID 5842390420%

Reaction Steps

To a solution of methylhydroxylamine HCl salt (28 mg, 0.326 mmol) in anhydrous MeOH (8 mL) was added NaOMe (25 wt. % in MeOH, 15.83 mg, 0.294 mmol), followed by (E)-N-(6-hydroxy-2-phenylchroman-4-ylidene)cyanamide (86 mg, 0.326 mmol). After stirred 10 minutes, the solvent was removed in vacuum. The residue was dissolved in DCM (15 mL) and filtered, and the solvent was removed in vacuum to give the crude product, which was purified by preparative TLC to give 3′-amino-2′-methyl-2-phenyl-2′H-spiro[chroman-4,5′-[1,2,4]oxadiazol]-6-ol (20 mg, 20%). 1HNMR(CDCl3): 7.30-7.51 (m, 5H), 6.95 (s, 1H), 6.69 (m, 2H), 5.15 (t, 3H), 2.98 (s, 3H), 2.28 (d, 2H), 1.17 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450308B2
Source datasetuspto-grants-2013_05
ORD IDord-06e8702caeba41a78194119c843694e0
Source noteuspto-grants-2013_05