HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131588Generated: October 25, 2026
Bromine → 2-Bromo-4-cyclopentoxy-3-hydroxy-benzaldehyde
https://huagongshe.com/reaction/131588
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 4-Cyclopentyloxy-3-hydroxybenzaldehyde | HCID 16726149 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Bromo-4-cyclopentoxy-3-hydroxy-benzaldehyde | HCID 21105707 | 58% |
Reaction Steps
4-cyclopentoxy-3-hydroxy-benzaldehyde (1.0 gm, 4.84 mmol) was dissolved in glacial acetic acid (20 ml). Anhydrous sodium acetate (0.8 gm, 9.7 mmol) was added to the above solution followed by powdered iron (0.022 gm). The system was flushed thoroughly with nitrogen. A solution of bromine (0.854 gm, 5.32 mmol) in glacial acetic acid (10 ml) was added to the above stirred suspension at 15° C. over a period of 15 min. The reaction mixture was stirred at 15° C. for 45 min. The reaction mixture was poured into aqueous 2% sodium bisulfite (100 ml) and stirred for 10 min. The precipitate was filtered washed with water (100 ml), and dried to obtain 800 mg of 2-bromo-4-cyclopentoxy-3-hydroxy-benzaldehyde as white powder mp: 107-109° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07384962B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-5424996d56024a2782ce8d3a48d3dd08 |
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| Source note | uspto-grants-2008_06 |
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