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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861617Generated: November 1, 2026

Hydrochloric Acid → HCID 17888762, compound

https://huagongshe.com/reaction/1861617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzyl BromideHCID 7498—
ReactantDiethyl (3-oxobutyl)phosphonateHCID 14033—
ReactantSodium hydrideHCID 24758—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
ProductHCID 17888762HCID 17888762—

Reaction Steps

250 ml of THF are added to a stirred suspension of 300 mmol of sodium hydride, which has been washed with n-pentane, and 280 mmol of 3-oxobutylphosphonic acid diethyl ester (1a) are added dropwise at room temperature. After 2 hours' stirring at constant temperature, the reaction mixture is cooled with an ice/common salt mixture and 1.3 equivalents of n-BuLi are added dropwise. After a further 2 hours' stirring at 0° C., 310 mmol of benzyl bromide (dissolved in 50 ml of THF) are slowly added. The mixture is allowed to rise to room temperature, stirred for a further 3 hours and combined with 20 ml of 1 molar HCl. The reaction solution is poured into iced water, extracted three times with 100 ml portions of chloroform and the combined organic phases are washed with saturated common salt solution. Purification of 1b performed chromatographically on silica gel with methylene chloride and ethyl acetate as mobile solvent. (Reaction conditions, c.f.: B. Resul, J. Stjernschantz, K. No, C. Liljebris, G. Selén, M. Astin, M. Karlsson, L. Z. Bito J. Med. Chem. 1993, 36, 243-248)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06534489B1
Source datasetuspto-grants-2003_03
ORD IDord-16535a1ceac64631b70bc4095ab40b3a
Source noteuspto-grants-2003_03