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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936560Generated: November 4, 2026

Hydrochloric Acid → HCID 10965199, compound

https://huagongshe.com/reaction/1936560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetic acid 10-acetoxymethyl-anthracen-9-ylmethyl esterHCID 613145—
Reactant1-Fluoro-4-(methylthio)benzeneHCID 3083565—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventWaterHCID 962—
SolventCarbon DisulfideHCID 6348—
ProductHCID 10965199HCID 1096519958%

Reaction Steps

A mixture of 4-fluorothioanisole (19c) (4 g, 28.13 mmol), anhydrous aluminium chloride (8.40 g, 63.02 mmol) and carbon disulphide (89 ml) was heated at reflux under argon atmosphere, and acetic arhydride (2.65 ml, 28.07 mmol) was added dropwise in 2 h. After refluxing for 24h, the solution was poured into crushed ice, water (62.48 ml) and concentrated hydrochloric acid (2.68 ml). The organic phase was separated and water extracted with dichloromethane (3×30 ml), the organic layers were washed with brine, dried and concentrated. The oily residue was chromatographed (50% petroleum ether 40-60° in dichloromethane) to afford 20c (2.98 g) as a colourless crystalline solid, mp 82.0-84.3° C. (58% yield). 1H NMR (CDCl3) δ7.49-7.43 (dd, 1H, J=9.23, 2.44 Hz); 7.29-7.11 (m, 2H); 2.57 (s, 3H); 2.39 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06391870B2
Source datasetuspto-grants-2002_05
ORD IDord-384ccae2082740e484f405853a213b02
Source noteuspto-grants-2002_05