HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromobenzaldehyde → 1-(2-Bromophenyl)-1-propanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromobenzaldehyde | HCID 81129 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(2-Bromophenyl)-1-propanol | HCID 13444279 | 102.3% |
Reaction Steps
A solution of 2-bromobenzaldehyde (1.85 g, 10 mmol) in THF (30 mL) at −70° C. was treated with 3 M solution of ethylmagnesium bromide (3.5 mL, 10.5 mmol). The mixture was warmed to room temperature for 6 hours and quenched with saturated solution of NH4Cl. The mixture was extracted with ethyl ether to provide the crude alcohol (yield: 2.2 g; ˜100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06472416B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-cabfe51b5f1c44e6bf266c751376711f |
| Source note | uspto-grants-2002_10 |