Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648756Generated: October 31, 2026

Carbofuran → 82560-28-9

https://huagongshe.com/reaction/1648756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbofuranHCID 2566—
ReactantTriethylamineHCID 8471—
ReactantSulfur dichlorideHCID 25353—
ReactantDiethyl 3,3'-IminodipropionateHCID 352310—
SolventDichloromethaneHCID 6344—
Product82560-28-9HCID 3067957—

Reaction Conditions

Temperature0 °C

Reaction Steps

A 11 g quantity (0.05 mole) of 2,3-dihydro-2,2-dimethylbenzofuran-7-yl N-methyl-carbamate was dissolved in 70 ml of methylene chloride, 5.2 g (0.05 mole) of sulfur dichloride was added to the solution with cooling, and 5 g (0.05 mole) of triethylamine was further added dropwise to the solution at -10° to -5° C. The mixture was stirred at 0° C. for one hour and further at room temperature for 2 hours. After cooling to -10° to -5° C., 10.9 g (0.05 mole) of diethyl iminodipropionate was added dropwise to the mixture, and 5 g (0.05 mole) of triethylamine was further added dropwise to the mixture. The resulting mixture was stirred at 0° C. for 2 hours and thereafter allowed to stand overnight at room temperature. With addition of 100 ml of methylene chloride, the reaction mixture was washed with 100 ml of water three times. The methylene chloride layer was dried and then concentrated in a vacuum to give an oily product, which was almost entirely composed of the desired product although containing small amounts of impurities. Yield: 16.9 g (72.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04413005
Source datasetuspto-grants-1983_11
ORD IDord-382ad3f33da24f0991db285b430dd01f
Source noteuspto-grants-1983_11