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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071576Generated: October 27, 2026

Hydrochloric Acid → 8-Oxatricyclo[7.4.0.0,2,7]trideca-1(9),2(7),3,5,10,12-hexaene-5-sulfonyl chloride

https://huagongshe.com/reaction/1071576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfur DioxideHCID 1119—
Reactant3-DibenzofuranamineHCID 20061—
ReactantSodium NitriteHCID 23668193—
CatalystCupric ChlorideHCID 24014—
SolventAcetic AcidHCID 176—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Product8-Oxatricyclo[7.4.0.0,2,7]trideca-1(9),2(7),3,5,10,12-hexaene-5-sulfonyl chlorideHCID 22179305—

Reaction Steps

3-Aminodibenzofuran (10 g, 54.6 mol) was diazotized by dissolving in 180 mL glacial acetic acid, 50 mL water, and 14 mL concentrated hydrochloric acid at 0° C. and adding 15 mL of a 5.5 M aqueous solution of sodium nitrite. The resulting mixture was stirred for 1 hour before pouring into a solution of copper(II)chloride (2.0 g, 14.9 mmol) in 240 mL of a 1:1 mixture of benzene and glacial acetic acid saturated with sulfur dioxide. This mixture was allowed to warm to room temperature and stirred for 16 hours. The reaction was partitioned between water and chloroform. The chloroform layer was washed with water, dried over magnesium sulfate, filtered, and concentrated to give the title compound as a yellowish solid; melting point=142-144° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06906092B2
Source datasetuspto-grants-2005_06
ORD IDord-85d5e1884c8d44ecb394c4dae678537b
Source noteuspto-grants-2005_06