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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458795Generated: October 26, 2026

Water → 5-(3,4-Dimethoxy-benzyl)-7,8-dimethoxy-2,3,4,5-tetrahydro benzo[f][1,4]oxazepine

https://huagongshe.com/reaction/458795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium borohydrideHCID 4311764—
ReactantN-[2-(3,4-Dimethoxy-phenoxy)-ethyl]-2-(3,4-dimethoxy-phenyl)-acetamideHCID 18442595—
SolventAcetonitrileHCID 6342—
SolventDichloromethane methanolHCID 21226129—
Product5-(3,4-Dimethoxy-benzyl)-7,8-dimethoxy-2,3,4,5-tetrahydro benzo[f][1,4]oxazepineHCID 1844258533.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of N-[2-(3,4-dimethoxy-phenoxy)-ethyl]-2-(3,4-dimethoxy-phenyl)-acetamide (3.6 g, 9.56 mmol) in dry CH3CN (20 ml), was added POCl3 (2.62 ml, 28.6 mmol). The resulting mixture was stirred at reflux for 3 h under nitrogen. After cooling, the reaction mixture was concentrated in vacuo and the residue was dissolved in MeOH (80 ml). The solution was cooled to 0° C. and NaBH4 (2.53 g, 67.0 mmol) was added portionwise. The resulting pale yellow suspension was stirred at RT for 16 h under nitrogen. The reaction mixture was poured into H2O and extracted three times with CH2Cl2. The combined organic phases were dried over anhydrous MgSO4, filtered and concentrated to give a crude oil. Flash chromatography (CH2Cl2/MeOH: 9/1) gave the title product (1.14 g, 33%) as a viscous brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192950B2
Source datasetuspto-grants-2007_03
ORD IDord-1d88122cc52d43edab68e513f252c823
Source noteuspto-grants-2007_03