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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296773Generated: October 25, 2026

Thionyl Chloride → HCID 86595906, compound

https://huagongshe.com/reaction/1296773

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3,5-Dimethoxy-4-methylbenzoic acidHCID 3764486—
ReactantHCID 86595905HCID 86595905—
CatalystDimethylformamideHCID 6228—
SolventBenzeneHCID 241—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 86595906HCID 86595906100%

Reaction Steps

DMF (2 drops) and thionyl chloride (0.080 mL, 1.1 mmol) were sequentially added to a suspension of 3,5-dimethoxy-4-methyl benzoic acid (0.0995 g, 0.507 mmol) in benzene (2 mL). The reaction mixture was heated at reflux for 2 h, and then concentrated. The residue was dissolved in dichloromethane (1 mL) and then added dropwise to a solution of compound 65c (0.144 g, 0.512 mmol) and TEA (0.2 mL, 1.4 mmol) in dichloromethane (1 mL). The reaction mixture was stirred overnight at rt. The mixture was diluted with ethyl acetate and washed with 0.1 N HCl (2×) and saturated sodium bicarbonate solution, dried, and concentrated to give compound 65d (0.233 g, 100%) as a yellow solid ESI-MS m/e 460.4 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07247654B2
Source datasetuspto-grants-2007_07
ORD IDord-8b8681b5c8754aa8a78b1315cb74837f
Source noteuspto-grants-2007_07