Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065214Generated: October 27, 2026

Sulfur Dioxide → 2,3-Dihydro-2,2-dimethyl-7-benzofuranyl (dibutylaminothio)methylcarbamate

https://huagongshe.com/reaction/1065214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfur DioxideHCID 1119—
ReactantCarbofuranHCID 2566—
ReactantTriethylamineHCID 8471—
ReactantAmidosulfenyl chloride, N,N-dibutyl-HCID 81031—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
Product2,3-Dihydro-2,2-dimethyl-7-benzofuranyl (dibutylaminothio)methylcarbamateHCID 13206391—

Reaction Conditions

Temperature9.5 °C

Reaction Steps

Sulfur dioxide was passed through 30.2 g of a 50% solution of dibutylaminosulfenyl chloride (0.077 mole) in hexane until the solution had gained 2.8 g (0.044 mole). 2,3-Dihydro-2,2-dimethyl-7-benzofuranyl methylcarbamate (98%, 15.5 g, 0.069 mole) was added followed by dropwise addition of triethylamine (12.4 g, 0.123 mole) over a period of 28 minutes with stirring. Stirring was continued for about 18 hours. The mixture was cooled to 9.5° C., 31 ml of water and 40 ml of hexane were added, and the layers were separated. The organic layer was concentrated to yield 27.4 g of 94% (by hplc) 2,3-dihydro-2,2-dimethyl-7-benzofuranyl (dibutylaminothio)methylcarbamate (98% chemical yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04329293
Source datasetuspto-grants-1982_05
ORD IDord-4f7817f34f5a41a79ea7f4d899bf9e84
Source noteuspto-grants-1982_05