HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243071Generated: October 31, 2026
N-Methoxy-N-methylacetamide → HCID 59208500, compound
https://huagongshe.com/reaction/2243071
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Methoxy-N-methylacetamide | HCID 537505 | — |
| Reactant | 1-(2-methoxyethyl)-1H-imidazole | HCID 14366840 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59208500 | HCID 59208500 | 82.4% |
Reaction Steps
A solution of 30 ml (75 mmol) of 2.5 M n-butyllithium in hexanes was added slowly to a solution of 8.48 g (61.3 mmol) 1-(2-methoxyethyl)-1H-imidazole (WO 2003055876 A1) in 200 ml THF cooled in a dry ice-acetone bath. After stirring 1 h, 8 ml (75 mmol) of N-methoxy-N-methylacetamide was added quickly, and the solution was allowed to warm to room temperature over 30 min. After quenching with aqueous NH4Cl, the mixture was diluted with water and extracted twice with EtOAc. The combined EtOAc layers were which washed with brine, dried over anhydrous MgSO4, and concentrated to give an oil that was chromatographed on silica gel (100% DCM followed by gradient elution to 50% EtOAc in DCM). The title compound (8.5 g) was obtained as a mobile oil. MS (ES) (M+H)+: 169 for C8H12CN2O2; NMR: 2.69 (s, 3H), 3.34 (s, 3H), 3.71 (m, 2H), 4.61 (m, 2H), 7.12 (s, 1H), 7.26 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07674801B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-4ecdeebc4a054d5c81976a3e356c1542 |
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| Source note | uspto-grants-2010_03 |
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