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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439935Generated: November 1, 2026

Dimethyl Sulfide → HCID 19046449, compound

https://huagongshe.com/reaction/1439935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantTriethylamineHCID 8471—
ReactantChlorosuccinimideHCID 31398—
Reactant4-(Tert-Butyl)-2-ChloroanilineHCID 521094—
SolventDichloromethaneHCID 6344—
ProductHCID 19046449HCID 19046449—

Reaction Conditions

Temperature-5 °C

Reaction Steps

4-t-Butyl-2-chloroaniline (30 g) was dissolved in dichloromethane (1.21) and the solution was cooled to -5° C. N-chlorosuccinimide (21.7 g) was added portionwise to the vigorously stirred solution and stirring was continued for 1 h. Dimethyl sulfide (35 ml) was added to the solution (-5° C.) and stirring was continued for a further 1 h. The solution was then cooled to -65° C. and triethylamine (27 ml) was added. This solution was allowed to warm to room temperature overnight. The solution was evaporated to half volume, washed with sodium hydroxide (1N), water and brine successively. The organic solution was dried and evaporated and the residue was purified on silica using hexane to 3% ether in hexane as eluant. This afforded the product (31.2 g) as a red oil. 1H NMR (CDCl3, 250 MHz) δ 1.27 (9H, s, (CH3)3), 1.99 (3H, s, SCH3 ), 3.69 (2H, s, CH2SCH3), 4.38 (2H, br s, NH2), 6.92 (1H, d, J=2.0 Hz, ArH), 7.21 (1H, d, J=2.0 Hz, ArH). MS (CI+) m/z 244 (M+ +1, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05496833
Source datasetuspto-grants-1996_03
ORD IDord-8ba57f399ec742878ffc403c0525a67b
Source noteuspto-grants-1996_03