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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540355Generated: October 29, 2026

Sulfuric Acid → HCID 21975858, compound

https://huagongshe.com/reaction/540355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantDichloromethaneHCID 6344—
ReactantDimethoxymethaneHCID 8020—
ReactantN-(3-Bromophenethyl)-4-methylbenzenesulfonamideHCID 21975863—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductHCID 21975858HCID 2197585890%

Reaction Steps

To a stirred solution of sulfuric acid (60% w/w, 20 g) in 32 mL of toluene at r.t. was added 7.60 g of N-[2-(3-bromo-phenyl)-ethyl]-4-methyl-benzenesulfonamide, followed by 32 mL of dimethoxymethane. The reaction mixture was heated over an oil bath set at 50° C. externally with stirring under nitrogen for 15 h. LC/MS: retention time=4.549 min, MS 366/368. TLC (DCM): SM Rf=0.35, product Rf=0.65. The reaction was complete as judged by TLC. The reaction mixture was cooled to r. t. and diluted with ether (100 mL). The two layers were separated and the aqueous layer was extracted with ether (25 mL). The combined ethereal solution was washed with water (25 mL), saturated sodium bicarbonate (25 mL) and brine (20 mL), sequentially. Then, the ethereal solution was dried over anhydrous granular potassium carbonate, filtered, and concentrated in vacuo. The crude product, a solid after standing, was re-crystallized from ether (75 mL) and pentane (100 mL). The material was collected by suction filtration and dried under vacuum to obtain 6.6 g (90%) of the title compound as a white crystalline solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871788B2
Source datasetuspto-grants-2014_10
ORD IDord-23fe108184c54e26af66f08245065ef1
Source noteuspto-grants-2014_10