HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872298Generated: October 29, 2026
N-Methoxy-N-methyl-2-phenylacetamide → HCID 66665381, compound
https://huagongshe.com/reaction/872298
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methoxy-N-methyl-2-phenylacetamide | HCID 10419762 | — |
| Reactant | HCID 58229900 | HCID 58229900 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 66665381 | HCID 66665381 | — |
Reaction Steps
A solution of 5-(4-bromo-phenyl)-2-oxa-4-aza-bicyclo[3.1.1]heptan-3-one (prepared according to WO2009/148916, 4 g) in dry THF (60 mL) was cooled to −78° C. and treated with n-BuLi (6.56 mL of a 2.5M solution in hexane) and stirred for 30 minutes at this temperature before addition of further n-BuLi (13.1 mL of a 2.5M solution in hexane). Stirring was continued at this temperature for 30 minutes before a solution of N-methoxy-N-methyl-benzeneacetamide (prepared according to US6407119B1, 4.6 g) in THF (10 mL) was added. After 10 minutes the reaction was quenched with saturated aqueous ammonium chloride solution, extracted with EtOAc and the combined organic phases washed with brine, filtered and concentrated. The residue was triturated with hexane/EtOAc to give the title compound which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975265B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-390350192f2947f3b4acc0ccb2377f88 |
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| Source note | uspto-grants-2015_03 |
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