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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170727Generated: October 31, 2026

Sodium hydride → HCID 70976335, compound

https://huagongshe.com/reaction/2170727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium ChlorideHCID 433294—
Reactant4-Iodobenzyl bromideHCID 954258—
ReactantDiethyl 2-(4-bromobenzyl)malonateHCID 10860456—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 70976335HCID 7097633584%

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixed liquid containing diethyl 4-bromobenzylmalonate (9.88 g, 30.0 mmol) and anhydrous N,N-dimethylformamide (12.0 mL) was added gradually at 0° C. to a mixed liquid containing sodium hydride (62 wt % in oil, 1.74 g, 45 mmol) and anhydrous N,N-dimethylformamide (18.0 mL). Following stirring of the resulting mixed liquid at this temperature for 30 minutes, a mixed liquid containing 4-iodobenzyl bromide (11.6 g, 39.0 mmol) and anhydrous N,N-dimethylformamide (30 mL) was added. The resulting mixed liquid was stirred at room temperature for 3 hours, and a saturated aqueous solution of ammonium chloride was then added to halt the reaction. The organic layer was separated from the mixed liquid, and the water layer was extracted with ethyl acetate. The thus obtained organic layer was washed with a saturated saline solution and then dried using anhydrous magnesium sulfate. The organic layer was filtered, the filtrate was concentrated under reduced pressure, to the thus obtained residue were added lithium chloride (5.09 g, 120 mmol), water (1.08 mL) and N,N-dimethylformamide (100 mL), and the resulting mixture was heated for 12 hours at 160° C. The thus obtained mixed liquid was cooled to room temperature, water (100 mL) was added, and the mixture was extracted with ethyl acetate. The thus obtained organic layer was dried using anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=70:1), yielding the title compound (4h) (11.9 g, 25.2 mmol) as a yellow liquid in a yield of 84%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051246B2
Source datasetuspto-grants-2015_06
ORD IDord-93e8642c16774cf4aaceb413b310bbff
Source noteuspto-grants-2015_06