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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714501Generated: October 31, 2026

Hydrochloric Acid → HCID 68719156, compound

https://huagongshe.com/reaction/1714501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhthalic AnhydrideHCID 6811—
Reactanto-FluorobenzaldehydeHCID 67970—
ReactantHCID 178420676HCID 178420676—
SolventWaterHCID 962—
ProductHCID 68719156HCID 6871915688.7%

Reaction Steps

Under nitrogen atmosphere, 1300 mL (2.60 mol, 1.00 eq) of 2.0M methylmagnesium chloride-tetrahydrofuran solution was cooled, and 322.7 g (2.60 mol, 1.00 eq) of 2-fluorobenzaldehyde was added while adjusting the inside temperature to −20 to +2° C., followed by stirring for 30 minutes under a cooled condition in iced water. Conversion of methylation was 99.9% by determination by gas chromatography. Subsequently, while adjusting the inside temperature to −22 to 0° C., 385.1 g (2.60 mol, 1.00 eq) of phthalic anhydride was added, followed by stirring at room temperature through the night. Conversion of acylation was 99% or greater by determination by 1H-NMR. 1300 mL (2.60 mol, 1.00 eq) of 2.0N hydrochloric acid was added to the reaction-terminated liquid, followed by extraction with 650 mL of toluene. The recovered organic layer was washed with 650 mL of brine, dried with anhydrous sodium sulfate, concentrated under reduced pressure, and vacuum dried, thereby obtaining 706.1 g of racemic 1-(2-fluorophenyl)ethyl alcohol phthalate half ester represented by the following formula,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795478B2
Source datasetuspto-grants-2010_09
ORD IDord-7896cd91c7df42ce943d717f2b6f71d6
Source noteuspto-grants-2010_09