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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602429Generated: October 27, 2026

Hydrochloric Acid → Venom

https://huagongshe.com/reaction/602429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Tetrahydrofuranylmethyl triflateHCID 21664529—
ReactantN-(1,5-dimethyl-1,3,5-triazinan-2-ylidene)nitramideHCID 135476318—
SolventDimethylformamideHCID 6228—
ProductVenomHCID 13577980353.4%

Reaction Steps

A mixture comprising 10.0 g of (tetrahydro-3-furanyl)methanol, 29.5 g of trifluoromethanesulfonic anhydride, 10.0 g of pyridine and 200 ml of dichloromethane was stirred for an hour at room temperature. Water was poured into the reaction solution to separate the organic layer, which was washed with 1 N hydrochloric acid, water and a saturated saline solution, dried, and concentrated to obtain 20 g of 3-tetrahydro-furanylmethyl triflate. 3.25 g of 60% sodium hydride were added to 12.5 g of 1,5-dimethyl-2-nitroiminohexahydro-1,3,5-triazine and 60 ml of DMF at room temperature, followed by stirring for an hour. 20.0 g of the 3-tetrahydrofuranylmethyl triflate were added thereto, and the mixture was stirred at 50° C. for 2 hours. After cooling the mixture to room temperature, 50 ml of 2N hydrochloric acid were added thereto, followed by stirring at 50° C. for 2 hours. The resultant mixture was neutralized with sodium bicarbonate and extracted with dichloromethane, and the extract was dried and concentrated. The residue thus obtained was purified by silica gel column chromatography (eluent: 1:1 ratio of ethyl acetate/hexane) to obtain 7.8 g of 1-{(tetrahydro-3-furanyl)methyl}-2-nitro-3-methylguanidine (dinotefuran).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906535B2
Source datasetuspto-grants-2011_03
ORD IDord-c3a4dd43f57249b7b6a8d2b88c461a9d
Source noteuspto-grants-2011_03