Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186781Generated: November 3, 2026

2-Phenylethanol → 3-Chloro-6-phenethyloxypyridazine

https://huagongshe.com/reaction/1186781

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PhenylethanolHCID 6054—
ReactantSodium hydrideHCID 24758—
Reactant3,6-DichloropyridazineHCID 67331—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product3-Chloro-6-phenethyloxypyridazineHCID 43128056—

Reaction Steps

3,6-Dichloropyridazine (1.0 g, 6.712 mmol), 2-phenylethanol (820 mg, 6.712 mmol) and sodium hydride (60 percent suspension in oil, 268 mg, 6.712 mmol) were stirred in 25 ml of N-methylpyrrolidin-2-one at room temperature for 30 minutes. After concentrating, water and ethyl acetate were added, and the organic phase was removed, concentrated and purified by preparative HPLC (PR18, acetonitrile/water 0.1% TFA). Yield: 878 mg (56%), M+H+: 235.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673917B2
Source datasetuspto-grants-2014_03
ORD IDord-050a1149c3394e89821c411c6e8ed14e
Source noteuspto-grants-2014_03