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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | Carbofuran | HCID 2566 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Amidosulfenyl chloride, N,N-dibutyl- | HCID 81031 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2,3-Dihydro-2,2-dimethyl-7-benzofuranyl (dibutylaminothio)methylcarbamate | HCID 13206391 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04329293 |
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| Source dataset | uspto-grants-1982_05 |
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| ORD ID | ord-4f7817f34f5a41a79ea7f4d899bf9e84 |
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| Source note | uspto-grants-1982_05 |
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