HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1464815Generated: November 1, 2026
Benzyl Bromide → p-(Benzyloxy)phenethyl alcohol
https://huagongshe.com/reaction/1464815
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Tyrosol | HCID 10393 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | p-(Benzyloxy)phenethyl alcohol | HCID 3017260 | — |
Reaction Steps
To a solution of 4-hydroxyphenethyl alcohol (33 g, 0.24 mol) in dry dimethylformamide (200 ml), cooled to 0° C., was added potassium tert-butoxide (29 g, 0.26 mol) by portions. After 10 minutes, benzyl bromide (41 g, 0.28 mol) was added slowly. The reaction mixture was stirred for 15 minutes at 0° C., then for 3 hours at room temperature and was quenched with water (200 ml). The precipitate was collected, dried and recrystallized from isopropyl ether/hexanes (34 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05306726 |
|---|
| Source dataset | uspto-grants-1994_04 |
|---|
| ORD ID | ord-22221002ad8b4b41905de3519618714f |
|---|
| Source note | uspto-grants-1994_04 |
|---|