HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 3-Bromo-5-(methoxymethyl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Bromo-5-(bromomethyl)benzonitrile | HCID 14567861 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Bromo-5-(methoxymethyl)benzonitrile | HCID 67979398 | — |
Reaction Steps
MeOH (0.088 mL, 2.18 mmol) was added to a slurry of NaH (45 mg, 1.13 mmol) in DMF (2 mL). When gas evolution ceased, a solution of 3-bromo-5-(bromomethyl)benzonitrile (see WO2009/100169; 240 mg, 0.87 mmol) in DMF (1 mL) was added. The reaction was quenched by adding aq. sat NH4Cl solution. The mixture was partitioned between toluene (5 mL) and water (3 mL). The toluene layer was collected, washed with water, dried over Na2SO4, and concentrated in vacuo. The crude product was dried at reduced pressure and used in the next step: GCMS (CI) m/z 226 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08415483B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-321f846e955640749df791f13e5f839e |
| Source note | uspto-grants-2013_04 |