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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594270Generated: November 1, 2026

Isopropyl iodide → 2-Fluoro-6-isopropoxybenzaldehyde

https://huagongshe.com/reaction/594270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
ReactantCesium carbonateHCID 10796—
ReactantPotassium CarbonateHCID 11430—
Reactant6-FluorosalicylaldehydeHCID 2737327—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product2-Fluoro-6-isopropoxybenzaldehydeHCID 86695615—

Reaction Steps

A mixture of commercially available 2-fluoro-6-hydroxybenzaldehyde (3.000 g; 21.40 mmol), 2-iodopropane (10.919 g; 64.20 mmol), K2CO3 (5.918 g; 42.80 mmol), and Cs2CO3 (1.395 g; 4.28 mmol) in anh. DMF (63 ml) was stirred at rt, under nitrogen, for 16 h. Et2O was added and the organic layer was washed with water, dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure affording 2-fluoro-6-isopropoxybenzaldehyde as a yellow oil. LC-MS (conditions A): tR=0.74 min.; [M+H]+: 183.15 g/mol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242970B2
Source datasetuspto-grants-2016_01
ORD IDord-71efddc98ecd4bc19242c58fbdebbae5
Source noteuspto-grants-2016_01