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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746425Generated: October 26, 2026

Bromine → 2-Bromo-4-cyclopentoxy-3-hydroxy-benzaldehyde

https://huagongshe.com/reaction/746425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium AcetateHCID 517045—
Reactant4-Cyclopentyloxy-3-hydroxybenzaldehydeHCID 16726149—
ReactantSodium BisulfiteHCID 23665763—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
Product2-Bromo-4-cyclopentoxy-3-hydroxy-benzaldehydeHCID 2110570758%

Reaction Conditions

Temperature15 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393846B2
Source datasetuspto-grants-2008_07
ORD IDord-440d5b77ad774f189e3bb95825adb5b0
Source noteuspto-grants-2008_07