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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594267Generated: November 4, 2026

3-Hydroxybenzaldehyde → HCID 15058630, compound

https://huagongshe.com/reaction/594267

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantPotassium CarbonateHCID 11430—
ReactantEthane, 1-fluoro-2-iodo-HCID 69804—
SolventDimethylformamideHCID 6228—
ProductHCID 15058630HCID 15058630—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of commercially available 3-hydroxybenzaldehyde (2.000 g; 16.40 mmol), 1-fluoro-2-iodoethane (3.849 g; 22.10 mmol), and K2CO3 (4.527 g; 32.80 mmol) in anh. DMF (30 ml) was heated to 70° C., under nitrogen, for 3 h. After cooling to rt, the reaction mixture was filtered over a pad of celite. Et2O was added and the organic layer was washed with water, dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure affording 3-(2-fluoroethoxy)benzaldehyde as a green oil. LC-MS (conditions A): tR=0.62 min.; no ionisation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-844ce76d774a4efa97ca79964e0ced1b
Source noteuspto-grants-2016_01