Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240311Generated: October 31, 2026

Hydrochloric Acid → Benzo(b)thiophene-2,3-dione

https://huagongshe.com/reaction/240311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantThiophenolHCID 7969—
ReactantOxalyl chlorideHCID 65578—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductBenzo(b)thiophene-2,3-dioneHCID 9730378%

Reaction Steps

To a solution of benzenthiol (1 ml, 9.7 mmol) in Et2O (30 ml) at 0° C. oxalyl chloride (0.94 ml, 10.7 mmol) was added dropwise. The mixture was stirred at room temperature for 1.5 hour, then, the solvent was evaporated under reduced pressure. The crude was dissolved in CH2Cl2 (40 ml) and a solution of AlCl3 (4.75 g, 35 mmol) in CH2Cl2 (32 ml) was added dropwise at 0° C. The mixture was stirred for 16 hours at room temperature, then, ice and 1M HCl were added until a clear mixture was obtained. After 1 hour, the phases were separated and the aqueous layer was extracted with CH2Cl2 (3×30 ml). The collected organic phases were dried over Na2SO4, filtered and evaporated, affording 18 (1.2 g, 78%) as orange solid that was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648076B2
Source datasetuspto-grants-2014_02
ORD IDord-5dd89baaeae94135a4053910e4ebf138
Source noteuspto-grants-2014_02