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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518937Generated: October 30, 2026

Water → 2,3,5-Triiodobenzyl mesylate

https://huagongshe.com/reaction/518937

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,3,5-Triiodobenzyl alcoholHCID 3495743—
SolventDichloromethaneHCID 6344—
Product2,3,5-Triiodobenzyl mesylateHCID 8668220584%

Reaction Conditions

Temperature0 °C

Reaction Steps

Mesyl chloride (0.6 ml, 8 mmol) was added dropwise to a suspension of 2,3,5-triiodobenzyl alcohol 1 (1.94 g, 4 mmol) in dry dichloromethane (30 ml) containing diisopropylethylamine (1.4 ml, 8 mmol) at 0° C. under dry nitrogen gas flow. The reaction mixture was stirred 1 h15 at 0° C., then cold H2O (40 ml) was added. The resulting aqueous phase was extracted with dichloromethane (10 ml). The combined organic extracts were washed with H2O (8 ml) then dried (Na2SO4), filtered and concentrated. The pale yellow solid was also washed with cold methanol (35 ml). 1.894 g of 2,3,5-triiodobenzyl mesylate in the form of a white clean solid was obtained in 84% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115230B2
Source datasetuspto-grants-2015_08
ORD IDord-b3c177c46c9440bfbfacdcf93b922d39
Source noteuspto-grants-2015_08