HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl 3-(2-bromoacetyl)-4-hydroxybenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-(Bromoacetyl)-4-hydroxybenzoic acid | HCID 13573514 | — |
| Product | Methyl 3-(2-bromoacetyl)-4-hydroxybenzoate | HCID 18175087 | — |
Reaction Steps
The compound obtained in Step B (27.4 mmol) is dissolved in 150 ml of MeOH, and 54.8 mmol of thionyl chloride are added dropwise in the cold state. The mixture is then stirred for 1 hour at ambient temperature and then for 2 hours at reflux. After evaporating off the methanol and the thionyl chloride, the oily residue is taken up in AcOEt, washed with water and then dried over MgSO4. The solvent is evaporated off under reduced pressure and the solid obtained is recrystallised.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06605632B1 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-3fc277248fe64cc3b768eaa488cbd63e |
| Source note | uspto-grants-2003_08 |