Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023855Generated: November 1, 2026

Acetone → HCID 67206335, compound

https://huagongshe.com/reaction/1023855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantThionyl ChlorideHCID 24386—
Reactant3-chloro-2,6-dihydroxybenzoic acidHCID 3653117—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventPotassium CarbonateHCID 11430—
ProductHCID 67206335HCID 6720633527%

Reaction Conditions

Temperature10 °C

Reaction Steps

To a solution of 5-chloro-2,6-dihydroxybenzoic acid (Doyle, F. P. J. Chem. Soc., 1963, p. 497-506) (500 mg, 2.65 mmol) in DME (2 mL) was added DMAP (16.2 mg, 0.13 mmol) and acetone (200.2 mg, 3.45 mmol). The solution was cooled to 10° C. and thionyl chloride (448 mg, 3.77 mmol) was added over 10 min. The solution was allowed to overnight. The solution was diluted with water and neutralized with solid K2CO3 and the aqueous phase was extracted w/EtOAc. The combined organic layers were washed with water, brine and dried (Na2SO4). The crude residue was purified by column chromatography on silica gel to afford the product as yellow solid (162 mg, 27% yield). 1H NMR: 1.74 (s, 6H), 6.44 (d, 1H, J=8.0 Hz), 7.48 (d, 1H, J=8.0 Hz), 10.83 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722720B2
Source datasetuspto-grants-2014_05
ORD IDord-70b74ac15ab64e2a8dd917adf25b2b53
Source noteuspto-grants-2014_05