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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064752Generated: October 30, 2026

Triethylamine → 2-[5-(3-Cyanophenyl)-1-benzofuran-2-yl]ethyl methanesulfonate

https://huagongshe.com/reaction/1064752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-[2-(2-Hydroxyethyl)-1-benzofuran-5-yl]benzonitrileHCID 11414365—
SolventDichloromethaneHCID 6344—
Product2-[5-(3-Cyanophenyl)-1-benzofuran-2-yl]ethyl methanesulfonateHCID 22274445—

Reaction Conditions

Temperature0 °C

Reaction Steps

The product from Example 112C (170 mg, 0.65 mmol) and triethylamine (100 μL, 0.72 mmol) were dissolved into CH2Cl2 (3 mL) and cooled to 0° C. The solution was treated with methanesulfonyl chloride (55 μL, 0.71 mmol), and after 10 minutes it was permitted to slowly warm to room temperature. More methanesulfonyl chloride (10 μL, 0.13 mmol) and triethylamine (10 μL, 0.072 mmol) were added. The mixture was stirred until the reaction was nearly complete and then washed consecutively with water and brine, dried (Na2SO4), concentrated, and used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969730B2
Source datasetuspto-grants-2005_11
ORD IDord-078f21fd452e4f7cb8fbb7cedb7d7682
Source noteuspto-grants-2005_11