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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | N-[2-(3,4-Dimethoxy-phenoxy)-ethyl]-2-(3,4-dimethoxy-phenyl)-acetamide | HCID 18442595 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | 5-(3,4-Dimethoxy-benzyl)-7,8-dimethoxy-2,3,4,5-tetrahydro benzo[f][1,4]oxazepine | HCID 18442585 | 33.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192950B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-1d88122cc52d43edab68e513f252c823 |
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| Source note | uspto-grants-2007_03 |
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