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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1965921Generated: October 29, 2026

Hydrochloric Acid → 2-Formyl-6-phenylphenol

https://huagongshe.com/reaction/1965921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
Reactant(1,1'-Biphenyl)-2-olHCID 7017—
ReactantHCID 178418573HCID 178418573—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
Product2-Formyl-6-phenylphenolHCID 1070310071%

Reaction Steps

To 100.6 mmol of 2-phenyl phenol in 40 ml of tetrahydrofuran was added dropwise a 3-molar methylmagnesium bromide solution (36.7 ml; 110 mmol) in diethyl ether. After two hours of stirring at room temperature, gas evolution ceased. About 90% of the solvent were removed in vacuo and toluene (250 ml), triethylamine (20 ml), and paraformaldehyde (7.55 g; 251 mmol) were added. The mixture was heated to 88° C. and held at this temperature for two hours. After cooling down to room temperature, the yellow solution was introduced into cold hydrochloric acid (1M, 250 ml). The organic phase was separated and dried over sodium sulphate. After removal of the solvent in vacuo, 3-phenyl salicylaldehyde was recrystallized from ethanol at −20° C. Yield: 71%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420563B2
Source datasetuspto-grants-2013_04
ORD IDord-be0967dcf6084174bc09df1446d83b30
Source noteuspto-grants-2013_04