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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046814Generated: November 1, 2026

Lithium Hydroxide → 2-[2-(Benzhydrylidene-amino)-3-fluoropyridin-4-ylmethyl]-3-oxobutanoic acid ethyl ester

https://huagongshe.com/reaction/1046814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
ReactantSodium IodideHCID 5238—
ReactantEthyl AcetoacetateHCID 8868—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-Propanol, 2-methyl-, lithium salt (1:1)HCID 23664764—
Reactant[2-(Benzhydrylidene-amino)-3-fluoropyridin-4-yl]-methanolHCID 59139234—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-[2-(Benzhydrylidene-amino)-3-fluoropyridin-4-ylmethyl]-3-oxobutanoic acid ethyl esterHCID 59139286102.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of [2-(benzhydrylidene-amino)-3-fluoropyridin-4-yl]-methanol (compound 8c-4) (5g, 16.3 mmol), methanesulfonyl chloride (1.52 mL, 19.6 mmol) and lithium tert-butoxide (in THF) (18 mL, 18 mmol) in THF (40 mL) was stirred at 0° C. for 1 hour. The mixture was added to a solution of acetoacetic acid ethyl ester (4.16 mL, 32.7 mmol), lithium tert-butoxide (in THF) (19.6 mL, 19.6 mmol) and NaI (2.5 g, 16.3 mmol) in THF (18 mL). The solution was stirred at 50° C. for 3 hours, 0.2N LiOH (in water) and ethyl acetate were added thereto, and the solution was washed with 0.2N LiOH (in water) and saturated saline. After drying over anhydrous magnesium sulfate, the solvent was distilled away under reduced pressure to yield the title compound (6.98 g, quant.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569378B2
Source datasetuspto-grants-2013_10
ORD IDord-1b9acf59a09b4277ac4d542e4b7386f2
Source noteuspto-grants-2013_10