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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106734Generated: October 31, 2026

Pyridine → N-(2-benzyloxy-5-cyanomethoxy-phenyl)-methanesulfonamide

https://huagongshe.com/reaction/1106734

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(3-Amino-4-benzyloxy-phenoxy)-acetonitrileHCID 18789661—
SolventWaterHCID 962—
ProductN-(2-benzyloxy-5-cyanomethoxy-phenyl)-methanesulfonamideHCID 1878970846.3%

Reaction Steps

A solution of 5.9 g of (3-amino-4-benzyloxy-phenoxy)-acetonitrile and 24 ml of pyridine was cooled in an ice bath and treated at a dropwise rate with 3.46 g of methanesulfonyl chloride and stirred for 1 hour. The mixture was treated with 5 ml of water, removed the ice bath, and stirred at room temperature for 30 minutes. The mixture was poured into ethyl acetate, ice added, acidified with concentrated hydrochloric acid, washed with brine, dried (MgSO4), and evaporated. The residue was purified on silica gel eluting with ethyl acetate/hexane (2:5) and obtained 3.57 g of N-(2-benzyloxy-5-cyanomethoxy-phenyl)-methanesulfonamide as a cream solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057349
Source datasetuspto-grants-2000_05
ORD IDord-1a328153f73049618216d42a3f0b91f0
Source noteuspto-grants-2000_05