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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2251730Generated: November 2, 2026

Methanesulfonyl chloride → HCID 58880523, compound

https://huagongshe.com/reaction/2251730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 11536760HCID 11536760—
SolventDichloromethaneHCID 6344—
ProductHCID 58880523HCID 5888052316%

Reaction Steps

3 g (10 mmol) of [7-(4-nitrophenyl)-(5H,9H)-6,8-dioxabenzocyclohepten-2-yl]methanol in 50 ml of dichloromethane are introduced into a flask. 1.54 g (12 mmol) of diisopropylethylamine are added and 1.37 g (12 mmol) of mesyl chloride in solution in 10 ml of dichloromethane are added dropwise at −5° C. After 1 hour 30 minutes of reaction at −5° C., 20 ml of a 5% sodium bicarbonate solution are added, the phases are separated by decantation and the organic phase is washed with water. It is dried over sodium sulfate and the solvent is evaporated off. The crude product is purified by silica gel chromatography (heptane/ethyl acetate: 3/2) to give 0.6 g of methanesulfonic acid [7-(4-nitrophenyl)-(5H,9H)-6,8-dioxabenzocyclohepten-2-yl]methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07319155B2
Source datasetuspto-grants-2008_01
ORD IDord-931e0c223c094ea5bc8a05eeb78a8616
Source noteuspto-grants-2008_01