HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → HCID 22080505, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | 1-Naphthalenemethanamine | HCID 8355 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22080505 | HCID 22080505 | — |
Reaction Steps
A solution of 1-aminomethylnaphthalene (2.15 g, 13.6 mmol) and TEA (1.65 g, 16.3 mmol) in CH2Cl2 (50 mL) is treated with ethyl bromoacetate (2.28 g, 13.6 mmol) dropwise over 90 min. The mixture is stirred at RT for 3 h and washed with water. The organic layer is dried over anhydrous MgSO4 and concentrated. The residue is flash chromatographed on silica gel using CH2Cl2→1% MeOH in CH2Cl2 as the eluent to afford N-(1-naphthyl-methyl)-glycine ethyl ester as a yellow oil: [M+1]+=244.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07291635B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-5b7fa37eff5a4cb299db6a08c1df7799 |
| Source note | uspto-grants-2007_11 |