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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855951Generated: October 31, 2026

Water → alpha-Cyano-m-phenoxybenzyl mesylate

https://huagongshe.com/reaction/1855951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantBenzeneacetonitrile, alpha-hydroxy-3-phenoxy-, (alphaS)-HCID 93218—
SolventDiethyl EtherHCID 3283—
Productalpha-Cyano-m-phenoxybenzyl mesylateHCID 20482835—

Reaction Steps

α-Cyano-m-phenoxybenzyl alcohol (8.5 g, 38 mmol) is dissolved in 150 ml ether and cooled in an ice-bath. To the solution is slowly added methanesulfonyl chloride (5.4 g, 47 mmol) in 20 ml ether. After the mixture is stirred about 20 minutes, triethylamine (4.76 g, 47 mmol) in 20 ml ether is added slowly and the mixture kept at 0° for 24 hours. Water is then added and the organic layer is separated, washed with 30% aqueous sodium bisulfite and water, dried and solvent removed under vacuum to yield α-cyano-m-phenoxybenzyl mesylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04217302
Source datasetuspto-grants-1980_08
ORD IDord-5f6cc03fa67d45aa9ef8c74fbdb55c37
Source noteuspto-grants-1980_08