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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513239Generated: October 29, 2026

Benzaldehyde → HCID 117599874, compound

https://huagongshe.com/reaction/513239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantDiethyl EtherHCID 3283—
ReactantLithium ChlorideHCID 433294—
ReactantHCID 117599933HCID 117599933—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 117599874HCID 117599874—

Reaction Conditions

Temperature-10 °C

Reaction Steps

3M PhMgBr in diethyl ether (1.7 mL, 5.07 mmol, 1.1 eq.) is added dropwise to the solution of 4-Bromo-2-iodo-3-methyl-benzoic acid ethyl ester (1.7 g, 4.61 mmol), LiCl (195 mg, 4.61 mmol) in dry THF (50 mL) at −10° C. The mixture is stirred at −10° C. for 2 hours. Benzaldehyde (0.977 g, 9.22 mmol) is slowly added to mixture at −10° C. This solution is stirred at room temperature for 16 hours and diluted with saturated aqueous ammonium chloride solution (100 mL). This solution is extracted with ethyl acetate (3×70 mL). The combined organic layers are washed with water and brine, dried over anhydrous sodium sulfate, concentrated in vacuo. The residue is purified by a silica chromatography to give the desire compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102684B2
Source datasetuspto-grants-2015_08
ORD IDord-aaacb8f722bd4237a448338eb9c356eb
Source noteuspto-grants-2015_08