HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(ALLYLOXY)-5-BROMOBENZALDEHYDE → 5-Bromo-2-(2-propen-1-yloxy)benzenemethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(ALLYLOXY)-5-BROMOBENZALDEHYDE | HCID 2168706 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Bromo-2-(2-propen-1-yloxy)benzenemethanol | HCID 2194016 | 96.3% |
Reaction Steps
A solution of 2-allyloxy-5-bromobenzaldehyde (5.27 g, 21.9 mM) was treated with sodium borohydride, (0.415 g, 10.9 mM). The reaction was stirred at ambient temperature for 21/2 hours, water was added and the solvent removed at reduced pressure. The residue was acidified to pH 1 and extracted with ethyl acetate twice. The organic layers were combined, dried (MgSO4) and evaporated to give 2-allyloxy-5-bromobenzyl alcohol (5.12 g, 96%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06100258 |
| Source dataset | uspto-grants-2000_08 |
| ORD ID | ord-edc9e29f340046679bfad0cf545cd2e2 |
| Source note | uspto-grants-2000_08 |