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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906930Generated: October 29, 2026

Cyanic acid → Dibenzyl ether

https://huagongshe.com/reaction/1906930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanic acidHCID 540—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
ProductDibenzyl etherHCID 7657—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a slurry of 1.1 g of sodium hydride (21 mmole, 50% oil dispersion) in 25 ml of dry DMF at 0° C. was added a solution of 3.34 g of Example 1 Part G cyanoalcohol (20 mmole) in 10 ml of DMF over a period of 10 minutes. After stirring for an additional b 15 minutes, 3.6 g of benzyl bromide was added dropwise. The reaction mixture was stirred for 30 minutes at 0° C. and 3 hours at 25° C. then quenched with a saturated ammonium chloride solution, and diluted with ether. The organic layer was washed with brine. The combined aqueous layer was re-extracted with ether. The combined organic layer was dried over anhydrous MgSO4 and concentrated to leave an oil. The crude oil was chromatographed on a silica gel column, eluting with 10-20% ethyl acetate in hexanes to give 4.43 g of the title A benzyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04654366
Source datasetuspto-grants-1987_03
ORD IDord-206b7d427acc4bba9e6274272b6f6d73
Source noteuspto-grants-1987_03