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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441668Generated: October 30, 2026

Hydrochloric Acid → HCID 12525867, compound

https://huagongshe.com/reaction/441668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactanto-FluorobenzaldehydeHCID 67970—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 1-oxo-1,3-dihydro-2-benzofuran-5-carboxylateHCID 23299433—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 12525867HCID 12525867—

Reaction Steps

8.5 G. of 5-carbomethoxyphthalide and 2.43 g. of sodium methoxide were refluxed for 15 minutes in 250 ml of methanol, and then 5.55 g. of o-fluorobenzaldehyde was added. The mixture was refluxed for 20 hours and then poured into water and acidified with dilute hydrochloric acid. The solution was extracted with ethyl acetate and the extract washed, dried and evaporated. The residue was refluxed for 48 hours in 75 ml of acetic acid and 45 ml of 57% aqueous hydriodic acid containing 7.5 g. of red phosphorus. The mixture was poured into water and filtered. The residue was dissolved in ethanol and the solution filtered and evaporated to afford 2-(o-fluorophenethyl)benzene-1,4-dicarboxylic acid which was cyclized according to the method described in Example I, A to obtain 2-carboxy-9-fluoro-10,11-dihydro-5-oxo-5H-dibenzo[a,d]cycloheptene having a m.p. of 248.5° to 249.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04041173
Source datasetuspto-grants-1977_08
ORD IDord-7e40f12802874dbd9121ec747b51adc0
Source noteuspto-grants-1977_08