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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515915Generated: October 31, 2026

Dichloromethane → HCID 16093753, compound

https://huagongshe.com/reaction/515915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantCyanogen BromideHCID 10476—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 14962127HCID 14962127—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
ProductHCID 16093753HCID 16093753—

Reaction Conditions

Temperature0 °C

Reaction Steps

Aluminium chloride (19.4 g, 0.15 mol) is added all at once to a solution of 3-methyl-1-(4-methylbenzenesulphonyl)-1H-pyrrole (13.0 g, 55.3 mmol) in 1,2-dichloroethane (230 mL) at ambient temperature. After stirring for 20 minutes, cyanogen bromide (11.11 g, 0.10 mol) is added in portions over a period of 20 minutes. After 4.5 hours, an additional amount of cyanogen bromide (1.94 g, 18.3 mmol) is added. After stirring for 17 hours at ambient temperature, the reaction mixture is poured slowly into a mixture of dichloromethane (300 mL) and water (600 mL) cooled to 0° C. The resulting mixture is stirred for 1 hour. Subsequently the phases are separated and the aqueous phase is extracted with dichloromethane (3×150 mL). The combined organic phases are washed with water (2×150 mL) and brine (150 mL). The organic phase is dried over Na2SO4, filtered and concentrated in vacuo to obtain the expected compound in the form of a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108983B2
Source datasetuspto-grants-2015_08
ORD IDord-e6cd9a5bb4e74e37b8ede942b628e1ec
Source noteuspto-grants-2015_08