HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl bromide → Formamide, N-[2-[3-methoxy-4-(2-propynyloxy)phenyl]ethyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | N-[2-(4-hydroxy-3-methoxyphenyl)ethyl]formamide | HCID 11389958 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Formamide, N-[2-[3-methoxy-4-(2-propynyloxy)phenyl]ethyl]- | HCID 11379286 | — |
Reaction Steps
Sodium methoxide (32 ml of a 5.4 M solution in methanol, 0.17 mol) is added to a solution of N-[2-(4-hydroxy-3-methoxy-phenyl)-ethyl]-formamide (32 g, 0.16 mol) in methanol (400 ml). Propargyl bromide (20 g, 0.17 mol) is added and the mixture is refluxed for 4 hours. After evaporation the residue is taken up in ethyl acetate (400 ml) and washed with water (2×200 ml). The organic layer is dried over magnesium sulfate and evaporated. The residue is submitted to flash-chromatography to give the N-[2-(3-methoxy-4-prop-2-ynyloxy-phenyl)-ethyl]-formamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07700522B2 |
| Source dataset | uspto-grants-2010_04 |
| ORD ID | ord-9e383e7cf7b6404183fae35c03c5e9d0 |
| Source note | uspto-grants-2010_04 |