HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 19600927, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 13653220 | HCID 13653220 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19600927 | HCID 19600927 | 52.6% |
Reaction Steps
500 mg (1.8 mmol) of 5-methyl-5-(3-cyclopropylmethoxy-4-methoxyphenyl)-2-oxazolidinone was first agitated with 75 mg (3.1 mmol) of sodium hydride in 17 ml of dimethylformamide for 30 minutes and, after adding 0.32 ml (2.7 mmol) of benzyl bromide, for 2 hours at room temperature. The procedure was continued analogously to Example 10, thus obtaining 348 mg of 5-methyl-5(3-cyclopropylmethoxy-4-methoxyphenyl)-3-benzyl-2-oxazolidinone as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05783591 |
| Source dataset | uspto-grants-1998_07 |
| ORD ID | ord-14292947720444b6b633da07e5e68558 |
| Source note | uspto-grants-1998_07 |