Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503208Generated: October 30, 2026

Tetrahydrofurfuryl alcohol → [1,4]Benzodioxino[2,3-c]pyridazin-3-ylmethanol

https://huagongshe.com/reaction/1503208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofurfuryl alcoholHCID 7360—
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl[1,4]benzodioxino[2,3-c]pyridazine-3-carboxylateHCID 117695404—
SolventWaterHCID 962—
Product[1,4]Benzodioxino[2,3-c]pyridazin-3-ylmethanolHCID 11769116166.6%

Reaction Steps

To methyl[1,4]benzodioxino[2,3-c]pyridazine-3-carboxylate (950 mg) was added a mixed solvent of tetrahydrofuran-methanol (1:1) (20 ml), and the mixture was stirred under ice-cooling. To the mixture was added sodium borohydride (450 mg), and the mixture was stirred at 0° C. for 2 hr. Water was added and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was concentrated under reduced pressure, and the residue was washed with water to give [1,4]benzodioxino[2,3-c]pyridazin-3-ylmethanol (560 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212147B2
Source datasetuspto-grants-2015_12
ORD IDord-e2de03019b254c189317c4774b40a54c
Source noteuspto-grants-2015_12