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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182246Generated: November 3, 2026

Sodium Hydroxide → (1-Methyl-5-phenyl-1H-pyrazol-3-yl)methanol

https://huagongshe.com/reaction/2182246

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
ReactantCalcium ChlorideHCID 5284359—
ReactantEthyl 1-methyl-5-phenyl-1H-pyrazole-3-carboxylateHCID 7537623—
SolventTetrahydrofuranHCID 8028—
Product(1-Methyl-5-phenyl-1H-pyrazol-3-yl)methanolHCID 14354447—

Reaction Steps

A stirred suspension of sodium borohydride (1.28 g) in dry tetrahydrofuran (80 mL) was treated with calcium chloride (1.88 g). The mixture was stirred for 1 hour then treated with a solution of ethyl 1-methyl-5-phenylpyrazol-3-ylcarboxylate (5.2 g, prepared according to the procedure described by Martins et al., J. Heterocycl. Chem. (1999), 36(1), 217-220) in dry tetrahydrofuran (40 mL). After stirring at room temperature for 3 days and at reflux temperature for 8 hours the mixture was treated with sodium hydroxide solution (50 mL, 1N). This mixture was stirred at room temperature for 1 hour, then evaporated to remove the organic solvents and then extracted three times with dichloromethane (140 mL). The combined extracts were washed with water, then dried over magnesium sulfate and then evaporated to give the title compound as a white solid, m.p. 95-99° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897207B2
Source datasetuspto-grants-2005_05
ORD IDord-43d2396c043e4826ae81df7c2b846423
Source noteuspto-grants-2005_05