Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402723Generated: November 2, 2026

Benzyl Alcohol → HCID 44176641, compound

https://huagongshe.com/reaction/1402723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantSodium hydrideHCID 24758—
ReactantHCID 44178184HCID 44178184—
SolventDimethylformamideHCID 6228—
ProductHCID 44176641HCID 4417664183%

Reaction Steps

Sodium hydride (0.007 g, 0.18 mmol) was stirred in anhydrous DMF (4 mL) under a nitrogen atmosphere, and benzyl alcohol (0.016 g, 0.15 mmol) was added. After 15 min., 3-chloro-6-[4-(3-piperidin-1-yl-propoxy)-phenyl]-pyridazine (0.05 g, 0.15 mmol) was introduced, and the reaction mixture was stirred at room temperature for 5 h. The precipitate was collected by filtration, washed with H2O (10 mL) and dried in vacuo to provide the title compound as a white solid (0.050 g, 83%), m.p. 138° C.; 1H NMR (CDCl3) 2.00 (m, 2H, —CH2—), 2.50 (m, 2H, —CH2—), 4.10 (m, 2H, —CH2—), 7.00 (d, 1H, C—H), 7.05 (d, 2H, Ar—H), 7.75 (d, 1H, C—H), 7.95 (d, 2H, Ar—H) HPLC retention time 2.612 mina.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912183B2
Source datasetuspto-grants-2014_12
ORD IDord-142d6defe7d34b22940a304f91acdf20
Source noteuspto-grants-2014_12