HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 5314864, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 2-Naphthaleneacetic acid | HCID 11393 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 5314864 | HCID 5314864 | 100.5% |
Reaction Steps
To a stirred solution of 2-naphthylacetic acid (1 g, 5.4 mmol) in acetonitrile (10 mL) were added DBU (0.97 mL, 6.4 mmol) and benzyl bromide (0.77 mL, 6.4 mmol). After 3 hours the mixture was concentrated, and the residue was taken up in ethyl acetate. The organic phase was washed with 10% citric acid, 10% NaHCO3 and brine, dried (MgSO4), and concentrated to give 2-naphthylacetic acid benzyl ester as a white solid (1.5 g, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06268365B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-175b47cdf9c1436d8cd87f3bda080a2d |
| Source note | uspto-grants-2001_07 |