HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → N-[4-(3-Fluoro-benzyloxy)-phenyl]-malonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | N-[4-(3-fluoro-benzyloxy)-phenyl]-malonamic acid methyl ester | HCID 10335956 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[4-(3-Fluoro-benzyloxy)-phenyl]-malonamide | HCID 10017779 | 51% |
Reaction Steps
99 mg (0.31 mmol) N-[4-(3-fluoro-benzyloxy)-phenyl]-malonamic acid methyl ester (example 1) is dissolved in a mixture of 0.5 ml tetrahydrofuran and 1.0 ml of aqueous ammonium hydroxide (25%). The reaction vessel is capped and kept at 60° C. for 2.5 h. The reaction mixture is cooled, evaporated to dryness and diluted with water. Filtration provides 48 mg (51%) of the title compound as a light yellow solid. MS: m/e=303.2 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06762320B2 |
| Source dataset | uspto-grants-2004_07 |
| ORD ID | ord-08ab74e0c2b549aa9401b0c0f718b0a4 |
| Source note | uspto-grants-2004_07 |