HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54593Generated: October 26, 2026
m-Chloroperbenzoic acid → 5-Bromo-2-methoxyphenol
https://huagongshe.com/reaction/54593
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 5-Bromo-2-methoxybenzaldehyde | HCID 90684 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5-Bromo-2-methoxyphenol | HCID 142228 | 96.4% |
Reaction Steps
A solution of 5-bromo-2-methoxybenzaldehyde (100 g, 0.46 mol) in CHCl3 (250 ml) was cooled with an ice bath and 3-chloroperoxybenzoic acid (50-60% purity) (146 g, 0.51 mol) in CHCl3 (1000 ml) added. The reaction mixture was allowed to warm slowly to room temperature and stirred for 72h. The white solid was filtered off and the filtrate concentrated in vacuo. The residue was dissolved in Et2O (200 ml) and washed with 1M sodium sulphite solution (2×200 ml) then NaHCO3 [half saturated] (3×200 ml). The ether layer was washed with 10% aqueous NaOH (3×100 ml) and the combined basic extract was acidified with concentrated hydrochloric acid and extracted with Et2O (3×100 ml). The combined organic extract was dried (MgSO4) and florisil (10 g) filtered and the solvent removed under reduced pressure to give the title compound (90 g) as a pate brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05622977 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-3545a78f35774655b3b2b131c75388e2 |
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| Source note | uspto-grants-1997_04 |
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