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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295566Generated: October 31, 2026

Triethylamine → 5-(2-(Methanesulfonyloxy)ethoxy)-2-methylquinazoline

https://huagongshe.com/reaction/1295566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 17965146HCID 17965146—
SolventDichloromethaneHCID 6344—
Product5-(2-(Methanesulfonyloxy)ethoxy)-2-methylquinazolineHCID 1796513999%

Reaction Steps

To a solution of 2-(2-methylquinazolin-5-yloxy)ethanol (0.330 g, 1.62 mmol) in dichloromethane (20 mL) and triethylamine (0.34 mL, 2.43 mmol) was added methane sulfonyl chloride (0.14 mL, 1.78 mmol) dropwise. The reaction mixture was allowed to stir at room temperature for 2 h. The reaction mixture was diluted with further dichloromethane and partitioned with saturated NaHCO3 aq. The organic phase was washed with brine, dried (MgSO4) and evaporated in vacuo to give the title compound as a cream solid (0.452 g, 99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244726B2
Source datasetuspto-grants-2007_07
ORD IDord-aa3cdca877bd4626a5425f756590395e
Source noteuspto-grants-2007_07