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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 908653Generated: October 30, 2026

Methanesulfonyl chloride → HCID 59366517, compound

https://huagongshe.com/reaction/908653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium AzideHCID 33557—
ReactantHCID 22006767HCID 22006767—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 59366517HCID 5936651780.3%

Reaction Steps

A mixture of 1.0 gram (0.003 mole) of 2-(4-(3,3-dichloroprop-2-enyloxy)-2,6-dichlorophenoxy)ethan-1-ol, 0.33 gram (0.0033 mole) of TEA and 0.37 gram (0.0032 mole) of methanesulfonyl chloride in 10 mL of methylene chloride was stirred at ambient temperature for two hours. The reaction mixture was diluted with 25 mL of methylene chloride and was washed first with 25 mL of water followed by 10 mL of a saturated aqueous sodium chloride solution. The organic phase was dried with magnesium sulfate, filtered and the filtrate concentrated under reduced pressure leaving an oil, which solidified upon standing. The solid was dissolved in 10 mL of DMSO to which 0.32 gram (0.005 mole) of sodium azide was added. The reaction mixture stirred at ambient temperature for about 18 hours at which time the reaction mixture was heated at 60° C. for one hour. The mixture was allowed to cool to ambient temperature, diluted with 25 mL of water and extracted with two 25 mL portions of ethyl acetate. The combined extracts were washed with 20 mL of an aqueous saturated sodium chloride solution, dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure providing 0.86 gram of the subject compound as a foam. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08017635B2
Source datasetuspto-grants-2011_09
ORD IDord-ab383ec2687f436c899d2c955a09aed9
Source noteuspto-grants-2011_09