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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501075Generated: October 26, 2026

Salicylaldehyde → 2-(2,2-Dibromovinyl)phenol

https://huagongshe.com/reaction/1501075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSalicylaldehydeHCID 6998—
ReactantTriethylamineHCID 8471—
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-(2,2-Dibromovinyl)phenolHCID 999367277.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of triphenylphosphine (10.5 g, 40 mmol), carbon tetrabromide (6.6 g, 20 mmol) and triethylamine (3.0 g, 30 mmol) in dichloromethane (10 mL) was added 2-hydroxy-benzaldehyde (1.62 g, 13 mmol), and the mixture temperature was maintained at around 0° C. during the addition. After the addition was completed, the reaction mixture was stirred at room temperature for 1 hour. After the reaction, the mixture was poured into water (200 mL). And then the mixture was extracted with ethyl acetate (200 mL), washed with water (200 mL). The organic phase was dried over anhydrous sodium sulfate, and then filtered. The filtrate was concentrated and the residue was purified by column chromatography (silica gel, ethyl acetate/petroleum ether=1:5) to give the pure product 2-(2,2-dibromovinyl)phenol as a pink solid (2.8 g, 76%). LRMS (M−H)−: calcd 275.9. found 275.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206128B2
Source datasetuspto-grants-2015_12
ORD IDord-6807387dc472492eab554fd2f239255e
Source noteuspto-grants-2015_12