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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444794Generated: November 2, 2026

2,4-Dichlorobenzaldehyde → HCID 11591151, compound

https://huagongshe.com/reaction/1444794

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DichlorobenzaldehydeHCID 13404—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 59776431HCID 59776431—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11591151HCID 11591151—

Reaction Steps

To a solution of Trifluoro-methanesulfonic acid 4-methyl-2-oxo-2H-chromen-7-yl ester (340 mg, 1.1 mmol) in dry THF (8 mL0 at −20° C. was added drop wise 1.0 M LiHMDS solution in THF (1.2 mL). After 30 minutes 2,4-dichloro-benzaldehyde (130 μL) was added slowly into the reaction mixture and the reaction-mixture was stirred for 1 hour. The reaction mixture was quenched with saturated aqueous ammonium chloride (10 mL) and extracted with ethyl acetate (50 mL). The organic layer was separated and dried over sodium sulfate, concentrated and purified on silica gel eluted with 30% ethyl acetate in hexanes to yield trifluoro-methanesulfonic acid 4-[2-(2,4-dichloro-phenyl)-2-hydroxy-ethyl]-2-oxo-2H-chromen-7-yl ester as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662975B2
Source datasetuspto-grants-2010_02
ORD IDord-4811488636004acda8361f8bb3aaa517
Source noteuspto-grants-2010_02