HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 2-(3-Benzyloxyphenoxy)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phenol, 3-(2-hydroxyethoxy)- | HCID 152273 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(3-Benzyloxyphenoxy)ethanol | HCID 12147048 | 79.4% |
Reaction Steps
To a solution of O-(2-Hydroxyethyl)resorcinol (4 g) and sodium hydroxide (1.04 g) dissolved in methanol (60 mL) was added benzyl bromide (4.44 g), and the resulting reaction mixture was stirred overnight. After this time, approximately 30 mL of the methanol was removed in vacuo, and the mixture was diluted with methylene chloride (100 mL). The organics were washed with water and aqueous 1N NaOH, dried, and concentrated to provide 2-(3-benzyloxyphenoxy)ethanol (5.03 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06806369B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-39e70c5d47ff499eb457287233bf9d7b |
| Source note | uspto-grants-2004_10 |