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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257736Generated: November 2, 2026

Dimethylformamide → HCID 20085211, compound

https://huagongshe.com/reaction/257736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantHCID 20085198HCID 20085198—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 20085211HCID 2008521161%

Reaction Steps

To a clear solution of 3-butyl-3-[(1,2,4-triazol-1-yl)methyl]-2(3H)-benzofuranone (5.0 g, 0.0184 mole) and dimethyl formamide (20 mL) in a 300 mL round bottom flask, potassium t-butoxide (6.2 g, 0.0553 mole) was added and the reaction mixture stirred at room temperature for 5 minutes before adding methyl iodide (3.2 g, 0.0221 m). The reaction mixture was stirred with heating at 40° C. for 1 hour and 1.0 g of water was added. The stirring was continued for an additional 2 hours at 40° C., before adding 100 mL of water and 100 mL of ethyl ether for work up. The organic phase was isolated and dried over magnesium sulfate, evaporated by rotary evaporator to afford 4.0 g of oily concentrate (yield 61%), Example 69 of Table 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05264415
Source datasetuspto-grants-1993_11
ORD IDord-fb623ab0bdc04eb28b894c2da5849026
Source noteuspto-grants-1993_11