Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624192Generated: October 25, 2026

Benzyloxyamine hydrochloride → N-[4-[(E)-phenylmethoxyiminomethyl]phenyl]-1,3-dihydroisoindole-2-carboxamide

https://huagongshe.com/reaction/624192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyloxyamine hydrochlorideHCID 102312—
ReactantSodium AcetateHCID 517045—
ReactantN-(4-formylphenyl)isoindoline-2-carboxamideHCID 86665079—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductN-[4-[(E)-phenylmethoxyiminomethyl]phenyl]-1,3-dihydroisoindole-2-carboxamideHCID 57510176—

Reaction Steps

In a 8 mL sealed vial was mixed N-(4-formylphenyl)isoindoline-2-carboxamide (50 mg, 0.188 mmol) in methanol (1 ml). A solution of O-benzylhydroxylamine hydrochloride (45.0 mg, 0.282 mmol) and sodium acetate (46.0 mg, 0.338 mmol) in water (1.000 ml) was then added and the reaction was stirred overnight at room temperature. The reaction was diluted with water and the product was extracted with dichloromethane. The organic layer was washed with brine, dried with sodium sulfate, decanted, and concentrated. Purification by chromatography provided the title compound. 1H NMR (400 MHz, DMSO-d6) δ ppm 8.55 (s, 1H), 8.21 (s, 1H), 7.65 (m, 2H), 7.50 (m, 2H), 7.44-7.28 (m, 9H), 5.14 (s, 2H), 4.78 (bs, 4H); MS (ESI(+)) m/e 372 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302989B2
Source datasetuspto-grants-2016_04
ORD IDord-896d25df927643b19a9b7cb285d8a101
Source noteuspto-grants-2016_04