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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622091Generated: October 31, 2026

Formaldehyde → 3-Bromo-2-hydroxybenzaldehyde

https://huagongshe.com/reaction/1622091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactant2-BromophenolHCID 7244—
ReactantTriethylamineHCID 8471—
ReactantMagnesium ChlorideHCID 5360315—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
Product3-Bromo-2-hydroxybenzaldehydeHCID 1091055569.2%

Reaction Steps

2-Bromophenol (2 g, 11.5 mmol) was dissolved in anhydrous acetonitrile (25 mL) and the solution was charged with anhydrous (<1.5% water) magnesium chloride (4.4 g, 46 mmol) and dry triethylamine (12.5 mL, 86.3 mmol). The mixture was stirred for minutes and paraformaldehyde (2.8 g, 92 mmol) was added. The mixture was heated to a gentle reflux for 1 to 3 hours and then cooled. The mixture was poured onto an ether/5% citric acid mixture and the ether layer separated. The ether layer was washed with water, brine, dried over anhydrous sodium sulfate and concentrated by evaporation. Product purified from the residue by chromatography on silica gel employing 30% ethyl acetate/hexanes to give 3-bromo-2-hydroxybenzaldehyde (1.6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778625B2
Source datasetuspto-grants-2014_07
ORD IDord-c9df68cf56d84ebf822f004f0c55548c
Source noteuspto-grants-2014_07