HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Cyanide → (5-Bromo-2-naphthalenyl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 1-Bromo-6-(bromomethyl)naphthalene | HCID 11324032 | — |
| Solvent | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Product | (5-Bromo-2-naphthalenyl)acetonitrile | HCID 19869673 | 99.1% |
Reaction Steps
A suspension of 5-bromo-2-bromomethylnaphthalene (4.50 g, 15 mmol) and NaCN (784 mg, 16 mmol) in 9:1 CH3CN/H2O (150 mL) was heated to reflux for 1 hour during which time the reaction mixture became homogeneous. The solution was cooled to room temperature and the volatiles removed in vacuo. The aqueous residue was partitioned between H2O (200 mL) and CH2Cl2 (200 mL). The aqueous phase was further washed with CH2Cl2 (1×200 mL) and the combined organic layers dried (Na2SO4) and concentrated in vacuo to give the product as a white solid (3.66 g, 99%). This material was of sufficient purity to be used as such without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04895861 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-c31b33663eb7486197f1f27d5a9411b6 |
| Source note | uspto-grants-1990_01 |