HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron tribromide → Ethyl 3-(bromomethyl)phenoxyacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Ethyl [3-(hydroxymethyl)phenoxy]acetate | HCID 18367402 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 3-(bromomethyl)phenoxyacetate | HCID 11459982 | — |
Reaction Steps
To a solution of 3-hydroxymethyl-1-ethoxycarbonylmethoxybenzene (1 g) in dichloromethane (10 ml) was added BBr3 (0.45 ml). After 1 hour, the solvent was evaporated in vacuo and the residue was dissolved in ethyl acetate. The organic layer was washed with NaHCO3 and brine. The dried solvent was evaporated in vacuo to give 3-bromomethyl-1-ethoxycarbonylmethoxybenzene (0.76 g). NMR (CDCl3, δ): 1.29 (3H, t, J=7 Hz), 4.24 (2H, d, J=7 Hz), 4.61 (2H, s), 5.00 (1H, d, J=3.0 Hz), 5.05 (1H, d, J=3.0 Hz), 6.7-7.1 (3H, m), 7.2-7.3 (1H, m)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05972965 |
| Source dataset | uspto-grants-1999_10 |
| ORD ID | ord-93b1b64c9a5a44ce8317c9d9c79cee76 |
| Source note | uspto-grants-1999_10 |